Prof. Dr. FATMA SILAN

Yayın Ağı

SCI, SSCI ve AHCI İndekslerine Giren Dergilerde Yayınlanan Makaleler

Expanding the Genetic and Phenotypic Spectrum of Mowat-Wilson Syndrome: A Study of 10 Turkish Patients With an Intrafamilial Recurrence Caused by First Intragenic Large Deletion

Kablan A., Aru E. E., Atar S., Gumus A. A., İli E. G., KAYHAN G., et al.

American Journal of Medical Genetics, Part A , cilt.197, sa.3, 2025 (SCI-Expanded)

Exploring and Expanding Secondary Findings Through Exome Sequencing in the Turkish Population

AKCAN M. B., CEYLAN KÖSE C., Müge Çelik K., TEKİN K., Kaya D., SILAN F.

Annals of Human Genetics , 2025 (SCI-Expanded)

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

Kim A. H., Sakin I., Viviano S., Tuncel G., Aguilera S. M., Goles G., et al.

Life science alliance , cilt.7, sa.10, 2024 (SCI-Expanded)

A case report of a patient with neurodevelopmental disorder with impaired speech and hyperkinetic movements: A biallelic variant in the ZNF142 gene

Kaya D., CEYLAN KÖSE C., AKCAN M. B., SILAN F.

American Journal of Medical Genetics, Part A , cilt.194, sa.9, 2024 (SCI-Expanded)

Evaluation of Smooth Muscle Myosin Heavy Chain Isoform Expressions in a Buried Penis

Kurtuluş Ş., Süzen A., Sılan F., Öztopuz R. Ö.

Journal of Pediatric Surgery , cilt.59, sa.8, ss.1526-1530, 2024 (SCI-Expanded)

Exploring genetic variants in congenital monosaccharide-disaccharide metabolism: Carrier ratios and phenotypic insights

AKCAN M. B., SILAN F.

Journal of Pediatric Gastroenterology and Nutrition , cilt.78, sa.6, ss.1251-1260, 2024 (SCI-Expanded)

Zihinsel engelli ve dismorfik yüz yapısına sahip Çanakkaleli bir ailede yeni bir BRPF1 varyantına bağlı anemi ve trombositopeni: Olgu sunumu ve literatürün gözden geçirilmesi

Kose C. C., Kaya D., Akcan M. B., Silan F.

AMERICAN JOURNAL OF MEDICAL GENETICS, PART A , cilt.191, sa.6, ss.2209-2214, 2023 (SCI-Expanded)

Evaluating of colchicine use patterns and attack frequency of familial Mediterranean fever patients in the COVID-19 pandemic

AKCAN M. B., Albuz B., Ozdemir O., SILAN F.

International Journal of Rheumatic Diseases , cilt.26, sa.5, ss.988-991, 2023 (SCI-Expanded)

Re-evaluation of Genetic Variants in Parkinson's Disease Using Targeted Panel and Next-Generation Sequencing

KABLAN A., SILAN F., Ozdemir O.

Twin research and human genetics : the official journal of the International Society for Twin Studies , cilt.26, sa.2, ss.164-170, 2023 (SCI-Expanded)

A new entity in the NARS2 variant: The first reported case of type 1 diabetes mellitus associated with the phenotype

ÇOKYAMAN T., Cetin H., DOĞAN D., SILAN F.

Journal of Tropical Pediatrics , cilt.69, sa.1, 2023 (SCI-Expanded)

Genetic influence on urinary vitamin D binding protein excretion and serum levels: a focus on rs4588 C>A polymorphism in the GC gene

Doğan D., Özcan E. G., Çakır D. Ü., Sılan F.

Frontiers in Endocrinology , cilt.14, 2023 (SCI-Expanded)

Melatonin receptor gene polymorphisms as a risk factor in patients with diabetic peripheral neuropathy

OCAK Ö., SILAN F., ŞAHİN E. M.

DIABETES-METABOLISM RESEARCH AND REVIEWS , cilt.38, sa.8, 2022 (SCI-Expanded)

New results for monogenic diabetes with analysis of causative genes using next-generation sequencing: a tertiary centre experience from Turkey

KARAKILIÇ E., SAYGILI E. S., SILAN F., Onduc G. G., Agcaoglu U.

International Journal of Diabetes in Developing Countries , cilt.42, sa.4, ss.703-712, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

DÜNDAR M., FAHRİOGLU U., Yildiz S. H., Bakir-Gungor B., TEMEL Ş. G., AKIN H., et al.

FUNCTIONAL & INTEGRATIVE GENOMICS , cilt.22, sa.3, ss.291-315, 2022 (SCI-Expanded) Sürdürülebilir Kalkınma

A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation

Dincsoy Bir F., SILAN F., Velickovic J., Berkay Akcan M. B., ÖZDEMİR Ö.

MOLECULAR SYNDROMOLOGY , cilt.13, sa.3, ss.254-260, 2022 (SCI-Expanded)

Diagnostic Utility of Array Comparative Genomic Hybridization in Children with Neurological Diseases

ÇOKYAMAN T., SILAN F.

FETAL AND PEDIATRIC PATHOLOGY , cilt.41, sa.1, ss.68-76, 2022 (SCI-Expanded)

Copy number variations in patients with idiopathic recurrent pregnancy loss: an array-CGH approach

Yildiz O., SILAN F., Karakaya T., Özdemir Ö.

Turkish Journal of Medical Sciences , cilt.52, sa.5, ss.1689-1696, 2022 (SCI-Expanded)

A New Mutation, Hb A(2)-Canakkale [delta 10(A7)Ala -> Val; HBD: c.32C > T], and Other Well-Known delta Variants Identified in a Selected Cohort with Low Hb A(2) Levels

KARAKAYA T., SILAN F., ÖZDEMİR Ö.

HEMOGLOBIN , cilt.46, sa.2, ss.87-90, 2022 (SCI-Expanded)

The comparison of telomere length in cancer patients: Plasma, whole blood and tumor tissue

Urfali M., Sılan F., Urfali F. E., Gürgen A., Özdemir Ö.

Medicine Science And The Law , cilt.2021104111721, sa.2021;10(4):1117-21, ss.1117-1121, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients *

ALBUZ B., ÖZDEMİR Ö., SILAN F.

CLINICAL NEUROLOGY AND NEUROSURGERY , cilt.202, 2021 (SCI-Expanded) Sürdürülebilir Kalkınma

Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey.

Uludağ A., UYSAL A., Uludağ A., Ertekin Y. H., Tekin M., KÜTÜK B., et al.

Balkan journal of medical genetics : BJMG , cilt.19, ss.29-34, 2016 (SCI-Expanded)

Prevalence and mutations of ß-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey.

ULUDAG A., UYSAL A., ULUDAG A., ERTEKİN Y. H., TEKİN M., KÜTÜK B., et al.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.19, sa.1, ss.29-34, 2016 (SCI-Expanded)

**The CYP4502D64 and6 alleles are the molecular genetic markers for drug response: implications in colchicine non-responder FMF patients**

Yalcintepe S., ÖZDEMİR Ö., SILAN C., Ozen F., ULUDAĞ A., CANDAN F., et al.

EUROPEAN JOURNAL OF DRUG METABOLISM AND PHARMACOKINETICS , cilt.41, sa.3, ss.281-286, 2016 (SCI-Expanded)

Vitamin D Receptor Gene BSMI, FOKI, APAI, and TAQI Polymorphisms and the Risk of Atopic Dermatitis

KILIÇ S., SILAN F., Hiz M. M., IŞIK S., OGRETMEN Z., ÖZDEMİR Ö.

JOURNAL OF INVESTIGATIONAL ALLERGOLOGY AND CLINICAL IMMUNOLOGY , cilt.26, sa.2, ss.106-110, 2016 (SCI-Expanded)

The relationship between C-reactive protein rs3091244 polymorphism and ankylosing spondylitis

Akbal A., REŞORLU H., Gokmen F., Savas Y., ZATERİ C., Sargin B., et al.

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES , cilt.19, sa.1, ss.43-48, 2016 (SCI-Expanded)

Tumour necrosis factor alpha, ınterleukin 10 and ınterleukin 6 gene polymorphisms of ıschemic stroke patients ın south Marmara region of Turkey

ÖZKAN A., SILAN F., ULUDAĞ A., DEGIRMENCI Y., ÖZIŞIK KARAMAN H. I.

INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY , cilt.8, sa.10, ss.13500, 2015 (SCI-Expanded)

Hyperimmunoglobulin D Syndrome: Case Report

Sen H., SILAN F., Binnetoglu E., Gunes F., Akurut C., ULUDAĞ A., et al.

ARCHIVES OF RHEUMATOLOGY , cilt.30, sa.3, ss.244-246, 2015 (SCI-Expanded)

Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia

Djurovic J., Stojkovic O., Ozdemir O., Silan F., Akurut C., Todorovic J., et al.

INTERNATIONAL JOURNAL OF IMMUNOGENETICS , cilt.42, sa.3, ss.190-194, 2015 (SCI-Expanded) Sürdürülebilir Kalkınma

Multiple Inherited Thrombophilic Gene Polymorphisms in Spontaneous Abortions in Turkish Population.

YALÇINTEPE S., ÖZDEMİR Ö., HACIVELİOĞLU S. Ö., Akurut Ç., ULUDAĞ A., COŞAR E., et al.

INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE , cilt.4, sa.2, ss.120-7, 2015 (SCI-Expanded)

Contribution of the STAT4 rs7574865 gene polymorphism to the susceptibility to otoimmune thyroiditis in healthy population and psoriatic subgroups

HIZ M. M., OĞUZ S., IŞIK S., ÖĞRETMEN Z., SILAN F.

CENTRAL EUROPEAN JOURNAL OF IMMUNOLOGY , cilt.40, sa.4, ss.437-441, 2015 (SCI-Expanded)

Bcii-RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Ozdemir O., Kayatas M., Cetinkaya S., YILDIRIM M. E., SILAN F., Kurtulgan H. K., et al.

RENAL FAILURE , cilt.37, sa.2, ss.292-296, 2015 (SCI-Expanded)

C-reactive protein gene and Toll-like receptor 4 gene polymorphisms can relate to the development of psoriatic arthritis

Akbal A., Oguz S., Gokmen F., Bilim S., REŞORLU H., SILAN F., et al.

CLINICAL RHEUMATOLOGY , cilt.34, sa.2, ss.301-306, 2015 (SCI-Expanded)

The Relationship between Obstructive Sleep Apnea Syndrome and Apolipoprotein E Genetic Variants

UYRUM E., Balbay O., Annakkaya A. N., Balbay E. G., SILAN F., Arbak P.

RESPIRATION , cilt.89, sa.3, ss.195-200, 2015 (SCI-Expanded)

Is the HLA B27 genotype a risc faktor for psoriatic arthritis and psoriasis vulgaris?

Ogretmen Z., Hiz M. M., SILAN F., Kosar S., ÖZDEMİR Ö.

TURKDERM-TURKISH ARCHIVES OF DERMATOLOGY AND VENEROLOGY , cilt.48, sa.3, ss.131-134, 2014 (SCI-Expanded)

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension.

ULUDAĞ A., SILAN F., Ozdemir O., Ogretmen Z., hiz m.

ANNALS OF SAUDI MEDICINE , cilt.34, sa.4, ss.340-345, 2014 (SCI-Expanded)

Two Siblings with Currarino Syndrome with 7q34 Deletion Due to Maternal t(7;14)(q34;p13)

Yildirim S., Topaloglu N., SILAN F., Kuru D.

HONG KONG JOURNAL OF PAEDIATRICS , cilt.19, sa.3, ss.181-184, 2014 (SCI-Expanded)

Variable R.Msp1 fragmentation in genomic DNA due to DNA hypomethylation in CRF patients with MTHFR C677T gene polymorphism: from genetics to epigenetics

ÖZDEMİR Ö., SILAN F., URFALI M., ULUDAĞ A., Arı E., Kayataş M.

GENE THERAPY AND MOLECULAR BIOLOGY , cilt.16, ss.77-87, 2014 (SCI-Expanded)

Association Between Inherited Thrombophilia and Impaired Right Ventricular Function in Deep Vein Thrombosis Without Symptomatic Pulmonary Embolism

AŞGÜN H. F., KIRILMAZ B., Saygi S., Ozturk O., SILAN F., KARATAĞ O., et al.

CLINICAL AND APPLIED THROMBOSIS-HEMOSTASIS , cilt.20, sa.3, ss.270-277, 2014 (SCI-Expanded)

Relationship between response to colchicine treatment and MDR1 polymorphism in familial Mediterranean fever patients.

ULUDAĞ A., SILAN C., Atik S., AKURUT Ç., ULUDAĞ A., SILAN F., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.18, sa.2, ss.73-6, 2014 (SCI-Expanded)

Relationship Between Response to Colchicine Treatment and MDR1 Polymorphism in Familial Mediterranean Fever Patients

ULUDAĞ A., SILAN C., Atik S., Akurut C., Uludag A., SILAN F., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.18, sa.2, ss.73-76, 2014 (SCI-Expanded)

The distribution of FV-Leiden, prothrombin and plasminogen activator inhibitor gene mutations in patients with obstructive sleep apnea.

Nihat Annakkaya A G. B. E. K. E. B. O., HIZ M. M., Sılan F.

Genet Couns. , cilt.25, sa.1, ss.69, 2014 (SCI-Expanded)

Endothelial function and germ-line ACE I/D, eNOS and PAI-1 gene profiles in patients with coronary slow flow in the Canakkale population: multiple thrombophilic gene profiles in coronary slow flow

GAZİ E., Temiz A., Altun B., BARUTÇU A., SILAN F., Colkesen Y., et al.

CARDIOVASCULAR JOURNAL OF AFRICA , cilt.25, sa.1, ss.9-14, 2014 (SCI-Expanded)

EFFECTS OF CYP2C19 AND P2Y12 GENE POLYMORPHISMS ON CLINICAL RESULTS OF PATIENTS USING CLOPIDOGREL AFTER ACUTE ISCHEMIC CEREBROVASCULAR DISEASE

Sen H. M., SILAN F., SILAN C., Degirmenci Y., Kamaran O. H.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.17, sa.2, ss.37-41, 2014 (SCI-Expanded)

Intercellular Adhesion Molecule-1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow

GAZİ E., BARUTÇU A., Altun B., Temiz A., Bekler A., Urfali M., et al.

MEDICAL PRINCIPLES AND PRACTICE , cilt.23, sa.4, ss.346-350, 2014 (SCI-Expanded)

Double Translocation: An Interesting Family History.

SILAN F., ÖZDEMİR Ö., UYSAL A., ULUDAĞ A., Erçelen N.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.1, ss.77-80, 2013 (SCI-Expanded)

The Proto-Oncogene KRAS and BRAF Profiles and Some Clinical Characteristics in Colorectal Cancer in the Turkish Population

OZEN F., ÖZDEMİR S., ZEMHERI E., HACIMUTO G., SILAN F., ÖZDEMİR Ö.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.17, sa.2, ss.135-139, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

DOUBLE TRANSLOCATION: AN INTERESTING FAMILY HISTORY

UYSAL A. O., ULUDAĞ A., SILAN F., Ercelen N., Zafer C., ÖZDEMİR Ö.

BALKAN JOURNAL OF MEDICAL GENETICS , cilt.16, sa.1, ss.77-80, 2013 (SCI-Expanded)

Possible Roles of the Xenobiotic Transporter P-glycoproteins Encoded by the MDR1 3435 C > T Gene Polymorphism in Differentiated Thyroid Cancers

ÖZDEMİR S., ULUDAĞ A., SILAN F., Atik S. Y., Turgut B., ÖZDEMİR Ö.

ASIAN PACIFIC JOURNAL OF CANCER PREVENTION , cilt.14, sa.5, ss.3213-3217, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G Variations in Breast Carcinoma

Ozen F., ERDİŞ E., Sik E., SILAN F., ULUDAĞ A., Ozdemir O.

ASIAN PACIFIC JOURNAL OF CANCER PREVENTION , cilt.14, sa.5, ss.2903-2908, 2013 (SCI-Expanded) Sürdürülebilir Kalkınma

Stria Gravidarum Is Genetic But Not Related With Collagen Gene Polymorphism

Gungor C. A. N., OĞUZ S., ULUDAĞ A., SILAN F., Gencer M., UYSAL A. O., et al.

GENE THERAPY AND MOLECULAR BIOLOGY , cilt.15, ss.131-137, 2013 (SCI-Expanded)

Does the maxillary sinus have a triggering role in nasal nitric oxide synthesis?

GÜÇLÜ O., ULUDAĞ A., AKÇALI A., Tekin K., ERDOĞAN H., SILAN F., et al.

RHINOLOGY , cilt.50, sa.4, ss.402-407, 2012 (SCI-Expanded)

**The prevalence of VKORC1 1639 G > A and CYP2C923 genotypes in patients that requiring anticoagulant therapy in Turkish population**

SILAN C., DOĞAN Ö. T., Silan F., Kukulguven F. M., AŞGÜN H. F., Ozdemir S., et al.

MOLECULAR BIOLOGY REPORTS , cilt.39, sa.12, ss.11017-11022, 2012 (SCI-Expanded)

Increased T allele frequency of 677 C>T polymorphism in the MTHFR gene in differentiated thyroid carcinoma.

SILAN F., ULUDAĞ A., ÖZDEMİR Ö., YALÇINTEPE S., ÖZDEMİR S., Erselcan T., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , sa.16, ss.780-784, 2012 (SCI-Expanded)

Increased T-Allele Frequency of 677 C > T Polymorphism in the Methylenetetrahydrofolate Reductase Gene in Differentiated Thyroid Carcinoma

ÖZDEMİR S., SILAN F., HASBEK Z., ULUDAĞ A., Atik S., Erselcan T., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.16, sa.7, ss.780-784, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Recurrent Pregnancy Loss and Its Relation to Combined Parental Thrombophilic Gene Mutations

ÖZDEMİR Ö., Yenicesu G. I., SILAN F., Koksal B., Atik S., Ozen F., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.16, sa.4, ss.279-286, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas

SILAN F., Gultekin Y., Atik S., Kilinc D., ALAN C., Yildiz F., et al.

MOLECULAR BIOLOGY REPORTS , cilt.39, sa.2, ss.1595-1599, 2012 (SCI-Expanded) Sürdürülebilir Kalkınma

Combined Effect of Factor V Leiden, MTHFR, and Angiotensin-Converting Enzyme (Insertion/Deletion) Gene Mutations in Hypertensive Adult Individuals: A Population-Based Study from Sivas and Canakkale, Turkey

DEMİREL Y., Dogan S., ULUDAĞ A., SILAN C., Atik S., SILAN F., et al.

GENETIC TESTING AND MOLECULAR BIOMARKERS , cilt.15, sa.11, ss.785-791, 2011 (SCI-Expanded) Sürdürülebilir Kalkınma

GJB2 35delG and Mitochondrial A1555G Mutations and Etiology of Deafness at the Gelibolu School for the Deaf in Turkey

SILAN F., GÜÇLÜ O., KADIOGLU L. E., SILAN C., ATIK S., ULUDAĞ A., et al.

JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY , cilt.7, sa.3, ss.361-371, 2011 (SCI-Expanded)

Association between ABCB1 (MDR1) Gene 3435 C > T Polymorphism and Colchicine Unresponsiveness of FMF Patients

Ozen F., SILAN C., ULUDAĞ A., CANDAN F., SILAN F., Ozdemir S., et al.

RENAL FAILURE , cilt.33, sa.9, ss.899-903, 2011 (SCI-Expanded)

Anophthalmia Cleft Lip Palate Absent Vomer Bone Nystagmus and Mental Motor Retardation A New Syndrome or Fryns Anophthalmia Plus Syndrome

ÖZÇELİK D., SAĞLAM İ., SILAN F., GEZEN G., ÜNVEREN T.

Cleft Palate-Craniofacial Journal , cilt.45, sa.3, ss.256, 2008 (SCI-Expanded)

A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN

Lehmann K., Seemann P., Silan F., Goecke T., Irgang S., Kjaer K., et al.

American Journal of Human Genetics , cilt.81, sa.2, ss.388-396, 2007 (SCI-Expanded)

Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate.

Senses D. A., Silan F., Uzun H., Alagöz D., Zafer C., Kocabay K., et al.

Genetic counseling (Geneva, Switzerland) , cilt.18, sa.2, ss.163-70, 2007 (SCI-Expanded)

Partial trisomy 1(q25qter) due to a de novo unbalanced 1;19 translocation in a neonate.

Senses D. A., Silan F., Uzun H., Zafer C., Ucar-Cavusoglu E., Kocabay K.

Genetic counseling (Geneva, Switzerland) , cilt.18, sa.4, ss.409-16, 2007 (SCI-Expanded)

Waardenburg syndrome in the Turkish deaf population.

Silan F., Zafer C., Onder I.

Genetic counseling (Geneva, Switzerland) , cilt.17, sa.1, ss.41-48, 2006 (SCI-Expanded)

Branchio-oculo-facial syndrome with the atresia of external ear

Ozturk O., Tokmak A., Demirci L., Silan F., Guclu E.

International Journal of Pediatric Otorhinolaryngology , cilt.69, sa.11, ss.1575-1578, 2005 (SCI-Expanded)

Congenital sialoblastoma (embryoma) associated with premature centromere division and high level of alpha-fetoprotein

Ozdemir I., Simsek E., Silan F., Demirci F.

Prenatal Diagnosis , cilt.25, sa.8, ss.687-689, 2005 (SCI-Expanded)

Non-Hodgkin's lymphoma and auricular hypoplasia: Associated with juvenile colloid milium or ligneous conjunctivitis?

Kavak A., Kaya M., Alper M., Çam M., Büyükbabani N., Bilen A., et al.

Journal of the European Academy of Dermatology and Venereology , cilt.19, sa.3, ss.348-351, 2005 (SCI-Expanded)

Evaluation of deaf children in a large series in Turkey

Ozturk O., Silan F., Oghan F., Egeli E., Belli S., Tokmak A., et al.

International Journal of Pediatric Otorhinolaryngology , cilt.69, sa.3, ss.367-373, 2005 (SCI-Expanded)

A novel L1CAM mutation with L1 spectrum disorders

Silan F., Ozdemir I., Lissens W.

Prenatal Diagnosis , cilt.25, sa.1, ss.57-59, 2005 (SCI-Expanded)

Syndromic etiology in children at schools for the deaf in Turkey

Silan F., Demirci L., Egeli A., Egeli E., Onder H. I., Ozturk O., et al.

International Journal of Pediatric Otorhinolaryngology , cilt.68, sa.11, ss.1399-1406, 2004 (SCI-Expanded)

Incontinentia pigmenti with NEMO mutation in a Turkish family

Silan F., Aydogan I., Kavak A., Bardaro T., D'Urso M.

International Journal of Dermatology , cilt.43, sa.7, ss.527-529, 2004 (SCI-Expanded)

SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism.

Borozdin W., Boehm D., Leipoldt M., Wilhelm C., Reardon W., Clayton-Smith J., et al.

Journal of medical genetics , cilt.41, sa.9, 2004 (SCI-Expanded)

A new mutation of the fukutin gene in a non-Japanese patient

Silan F., Yoshioka M., Kobayashi K., Simsek E., Tunc M., Alper M., et al.

Annals of Neurology , cilt.53, sa.3, ss.392-396, 2003 (SCI-Expanded)

Etiology of deafness at the Yeditepe School for the deaf in Istanbul

Egeli E., Çiçekci G., Silan F., Öztürk Ö., Harputluoǧlu U., Onur A., et al.

International Journal of Pediatric Otorhinolaryngology , cilt.67, sa.5, ss.467-471, 2003 (SCI-Expanded)

Protective effect of melatonin on β-cell damage in streptozotocin-induced diabetes in rats

Yavuz Ö., Cam M., BUKAN N., Guven A., Silan F.

Acta Histochemica , cilt.105, sa.3, ss.261-266, 2003 (SCI-Expanded)

Diğer Dergilerde Yayınlanan Makaleler

Spinal muscular atrophy carrier screening program: awareness and attitude of healthcare professionals in Turkey

Celik K. M., Kose C. C., KAYA D., TEKİN K., SILAN F.

Journal of Community Genetics , cilt.15, sa.6, ss.665-672, 2024 (ESCI)

Fragile-X-associated Tremor/Ataxia Syndrome (FXTAS) in a Female with FMR1 Premutation: Case Report

OCAK Ö., SILAN F.

İzmir Tepecik Eğitim Hastanesi Dergisi , cilt.32, sa.3, ss.488-491, 2022 (Hakemli Dergi)

Familial intragenic X-linked OPHN1 gene deletion in a newborn male infant with low birth weight and distinctive facial appearance that diagnosed by advanced microarray-CGH method

Aylanc H., Sılan F., Çokyaman T., Akcan M. B., Özdemir Ö.

Cumhuriyet Tıp Dergisi (ELEKTRONİK) , cilt.44, sa.1, ss.125-130, 2022 (Hakemli Dergi)

Interleukin-23R Gene Polymophisms in Patients with Diabetic Peripheral Polyneuropathy

OCAK Ö., SILAN F.

KONURALP TIP DERGISI , cilt.14, sa.2, ss.406-410, 2022 (ESCI)

Prognostic Prediction of BRCA Mutations by F-18-FDG PET/CT SUVmax in Breast Cancer

ÖZDEMİR S., SILAN F., Akgun M. Y., Araci N., Cirpan I., Ozturk F. K., et al.

MOLECULAR IMAGING AND RADIONUCLIDE THERAPY , cilt.30, sa.3, ss.158-168, 2021 (ESCI)

Investigation of TAp63 gene expression and follicle count using melatonin in cisplatin-induced ovarian toxicity

ŞAHİN H. Ö., DURAN M. N., SILAN F., SILAN E., SIDDIKOĞLU D., KILINÇ N.

International Journal of Research in Medical Sciences , cilt.9, sa.3, ss.658-664, 2021 (Hakemli Dergi)

Jinekolojik Kanserlerde Yeni Nesil DNA Dizi Analizi ile Saptanan Mutasyon Profilleri: Tek Merkez Vaka Serisi Sonuçlarımız

Şahin H., Özkan K., Albuz B., Sılan F.

Uludağ Üniversitesi Tıp Fakültesi Dergisi , cilt.46, ss.349-356, 2020 (Hakemli Dergi)

Çanakkale İlimizdeki Jinekolojik Kanserlerde Yeni Nesil DNA Dizi Analizi ile Saptanan Mutasyon Profilleri

ŞAHİN H. Ö., karacaer k. ö., ALBUZ B., SILAN F.

Uludağ Üniversitesi Tıp Fakültesi Dergisi , cilt.46, sa.3, ss.349-356, 2020 (Hakemli Dergi) Sürdürülebilir Kalkınma

Type-Specific Persistence/Clearance Results in Human Papillomavirus Infections in Turkish Women

DEMİR B., ŞAHİN H. Ö., Gülek B., SILAN F.

GORM:Gynecology Obstetrics & Reproductive Medicine , 2020 (Hakemli Dergi) Sürdürülebilir Kalkınma

Diagnostic outcomes for genetic testing of 54 genes in pregnancy loss using array CGH method: A two-year retrospective study Gebelik kayıplarında 54 genin array CGH methoduyla yapılan tanısal sonuçları: İki yıllık retrospektif çalışma

PAKSOY B., ÖZDEMİR Ö., SILAN F.

Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi , cilt.17, sa.4, 2020 (Hakemli Dergi)

Tedaviyi Etkileyen Tarama Testleri

KARAKAYA T., SILAN F., ÖZDEMİR Ö.

Türkiye Klinikleri Sağlık Bilimleri Dergisi , 2020 (Hakemli Dergi)

308G/A and 238G/A polymorphisms in the TNF-alpha gene may not contribute to the risk of arthritis among Turkish psoriatic patients

IŞIK S., SILAN F., KILIÇ S., Hiz M. M., Ogretmen Z., ÖZDEMİR Ö.

EGYPTIAN RHEUMATOLOGIST , cilt.38, sa.4, ss.313-317, 2016 (ESCI)

Hypermethylated promoter profiles for tumoursupressor APC p53 MSH6 and MGMT genes in CRCtumours

Şık E., ÖZDEMİR Ö., KÜÇÜK KURTULGAN H., URFALI M., SILAN F.

Pyrex Journal of Biomedical Research , 2016 (Hakemli Dergi)

An infertile case of 47 XYY syndromewithout autistic spectrum Cost effectivewell define of extra Y chromosome byGTG C bandings QF PCR and FISHanalyses

ÖZDEMİR Ö., PAKSOY B., Gürgen A., URFALI M., YILDIZ O., ULUDAĞ A., et al.

Cumhuriyet Tıp Dergisi , 2016 (Hakemli Dergi)

9qh liği Molar Gebelik İçin Bir Risk Faktörü mü

ÇAKIR GÜNGÖR A. N., SILAN F., KILINÇ N., GENCER M., ULUDAĞ A., COŞAR E., et al.

Jinekoloji - Obstetrik ve Neonatoloji Tıp Dergisi , 2016 (Hakemli Dergi)

Triploidy Diploidy Mosaisizm Diandry and Uniparental Isodisomy Fetus withOmphalocele and Contracted Finger

SILAN F., ÇAKIR GÜNGÖR A. N., URFALI M., ULUDAĞ A., ÖZDEMİR Ö.

Family Medicine & Medical ScienceResearch , 2015 (Hakemli Dergi)

Epileptik nöbet bulgusu ile gelen temporal kemik osteomu: Nadir bir olgu sunumu

GÜVEN M., AKMAN T., ARAS A. B., TOPALOĞLU N., ŞEN H. M., KILINÇ N., et al.

ODU Journal of Medicine , cilt.2015, sa.2, ss.83-86, 2015 (Hakemli Dergi)

PATAU SENDROMU, KOMPLET VEYA İNKOMPLET YAŞAM SÜRESİNDE ÖNEMLİ Mİ?

YILDIRIM Ş., TOPALOĞLU N., TEKİN M., SILAN F.

Anatol J Clin Investig , cilt.8, sa.4, ss.187-188, 2014 (Hakemli Dergi)

High Frequency of Chromosomal Anomalies and a Novel Chromosomal Insertion Associated with Infertility and Recurrent Miscarriages (Reproductive Failure) in West Turkey

Sılan F., Yalçıntepe S., Uysal D., Urfalı M., Uludağ A., Coşar E., et al.

GENE THERAPY AND MOLECULAR BIOLOGY , cilt.16, ss.139-148, 2014 (Hakemli Dergi)

Fetal Vegf Genotype is More Important for Abortion Risk than Mother Genotype

YALÇINTEPE S., SILAN F., HACIVELİOĞLU S. Ö., ULUDAĞ A., COŞAR E., ÖZDEMİR Ö.

INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE , cilt.3, ss.88-94, 2014 (ESCI)

Increased Sister Chromatid Exchanges in Patients with Gastrointestinal Cancers and in their First-Degree Relatives

Turgut T., Yaşar ., Yaykaşlı K. O., Ertaş E., SILAN F.

European Journal of Health Science , cilt.11, sa.2, ss.94, 2014 (Hakemli Dergi) Sürdürülebilir Kalkınma

Larenks Kanserli Hastalarımızda K-Ras Mutasyonları

KARA M., DEREKÖY F. S., GÜÇLÜ O., ÖZDEMİR Ö., SILAN F., BARUTÇU O., et al.

International Journal of Clinical Research , cilt.2, sa.1, ss.6-11, 2014 (Hakemli Dergi) Sürdürülebilir Kalkınma

Association of Vitamin D Receptor Gene Polymorphisms in Children With Atopic Diseases

TOPALOĞLU N., KILIÇ S., SILAN F., ULUDAĞ A., IŞIK S., çişem a.

GENE THERAPY AND MOLECULAR BIOLOGY , cilt.16, ss.55-60, 2014 (Scopus)

Characteristic findings of alstrom syndrome with a case report

SILAN F., GÜR S., KADIOGLU L. E., YALÇINTEPE S., ÜKİNÇ K., ULUDAĞ A., et al.

Journal of Clinical Diagnostics , sa.3, ss.75-77, 2013 (Hakemli Dergi)

Onsekiz Haftalık Spontan Olarak Sonlanan ve QF-PCR ile Saptanan Triploidik Fetus; Olgu Sunumu

YALÇINTEPE S., GENCER M., ULUDAĞ A., ÇAKIR GÜNGÖR A. N., KUMCULAR T., COŞAR E., et al.

International Journal of Clinical Research , cilt.1, ss.31-34, 2013 (Hakemli Dergi)

Tc-99m DMSA Scintigraphy in the Diagnosis of Renal Anomalies: A Turner Syndrome Case

ÖZDEMİR S., TAN Y. Z., TOPALOĞLU N., SILAN F., TEKİN M.

Turkiye Klinikleri Journal of Pediatrics , cilt.22, sa.1, ss.37-40, 2013 (Hakemli Dergi)

Fetal Anöploidi Açısından Yüksek Riskli Gebeliklerin QF-PCR İle Analizi

ÇAKIR GÜNGÖR A. N., HACIVELİOĞLU S. Ö., ULUDAĞ A., GENCER M., UYSAL A., Atik S., et al.

International Journal of Clinical Research , cilt.1, sa.1, ss.17-21, 2013 (Hakemli Dergi)

Tc 99 m DMSA scintigraphy in the diagnosis of renal anomalies A Turner case

ÖZDEMİR S., TAN Y. Z., SILAN F., TOPALOĞLU N.

Türkiye Klinikleri Pediatri Dergisi , cilt.22, sa.1, ss.37-40, 2013 (Hakemli Dergi)

Nöral tüp defekti gebeliği olan olguda terminasyon kararı

ÇAKIR GÜNGÖR A. N., GENCER M., YÜCESOY K., HACIVELİOĞLU S. Ö., KIZILDAĞ B., SILAN F.

Smyrna Tıp Dergisi , ss.27-30, 2012 (Hakemli Dergi)

A case of congenital muscular dystrophy similar to fukuyama-type with a missense mutation in the fukutin gene

Ozcetin M., Ates O., Kurt S., Firat M. M., SILAN F.

Journal of Pediatric Neurology , cilt.10, sa.1, ss.63-66, 2012 (Scopus)

Çok Sayıda Konjenital Anomalinin Eşlik Ettiği Trizomi 8 Mozaisizm Olgusu

SILAN F.

Turkiye Klinikleri Journal of Pediatrics , cilt.18, sa.4, ss.324-327, 2009 (Hakemli Dergi)

Waardenburg syndrome Waardenburg sendromu

Silan F., Zafer C.

SENDROM , cilt.17, sa.10, ss.57-61, 2005 (Scopus)

Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler

Reevaluation of Variants Of Uncertain Significance (VUS) in Familial Cancer Patients: Insights From Bioinformatic Reanalysis

Çelik K. M., Ceylan Köse C., Sılan F.

16. Ulusal Tıbbi Genetik Kongresi, Antalya, Türkiye, 4 - 08 Aralık 2024, ss.253

A Case of Diabetes Associated with a De Novo PAX4 Mutation and Concurrent SMAD6 Gene Mutation

KARAKILIÇ E., tufan c., CEYLAN KÖSE C., SAYGILI E. S., Talaibekova S., SILAN F.

Endobridge 2024, Antalya, Türkiye, 17 Ekim 2024

KERATİN 17 GEN MUTASYONUYLA İLİŞKİLİ AİLESEL STEATOKİSTOMA MULTİPLEKS OLGUSU

KESKİNKAYA Z., TEKİN K., IŞIK MERMUTLU S., KAYA Ö., ÇAKIR H., SILAN F.

11.Ulusal Pediatrik Dermatoloji Günleri, 23 - 26 Mayıs 2024

The Importance of Genetic Analysis in the Diagnosis of Complex Clinical MAnifestations:A case Report of Metabolic Rare Disease

CELİK K. M., KAYA D., KAMIŞ F., SILAN F.

8th INTERNATIONAL CONGRESS OF MEDICAL GENETICS, Kayseri, Türkiye, 21 Eylül 2023

EVALUATION OF GENETIC VARIANTS RELATED TO CONGENITAL MONOSACCHARIDE AND DISACCHARIDE METABOLISM DISORDERS FROM DATA OBTAINED BY WHOLE EXOME SEQUENCING, AND DETERMINATION OF CARRIER RATIOS IN ÇANAKKALE

AKCAN M. B., SILAN F.

14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Makedonya, 05 Ekim 2023

PEDIGREE ANALYSIS IN PROBANDS WITH VARIANTS IN THE CDH1 GENE

TEKİN K., Albay T. A., SILAN F.

14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Makedonya, 05 Ekim 2023

COMPOUND HETEROZYGOUS DCHR24 GENE VARIANTS IN DESMOSTEROLOSIS: A CASE REPORT WITH DEVELOPMENTAL DELAY AND CORPUS CALLOSUM AGENESIS

CEYLAN KÖSE C., AKCAN M. B., SILAN F.

14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Makedonya, 05 Ekim 2023

A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE

KAYA D., AKCAN M. B., CEYLAN KÖSE C., SILAN F.

14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Makedonya, 05 Ekim 2023

RETROSPECTIVE EVALUATION OF GENES RELATED TO FATTY ACID OXIDATION DEFECTS FROM WHOLE-EXOME SEQUENCING (WES) ANALYSIS WITH CURRENT DATA

SÖNMEZ V., SILAN F.

14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Makedonya, 05 Ekim 2023

A rare SLC6A1 gene variant in a family with intellectual disability: A case report from Çanakkale, Turkey

CEYLAN KÖSE C., ÇOKYAMAN T., SILAN F.

8.ULUSLARARASI ERCİYES TIP TIBBİ GENETİK KONGRESİ, Kayseri, Türkiye, 21 Eylül 2023

Dna Polimeraz Epsilon (POLE) Geninde Varyant Saptanan Hastalarda Genotip Fenotip Korelasyonu

Çelik K. M., Ceylan Köse C., Tekin K., Sılan F.

2. Ulusal HematoOnkoGenetik Kongresi / K.K.T.C., İskele, Kıbrıs (Kktc), 4 - 07 Mayıs 2023, ss.122

VHL geninde patojenik/muhtemel patojenik varyant saptanan olguların genotip-fenotip ilişkisi

Kaya D., Akcan M. B., Sönmez V., Sılan F.

2.Ulusal HematoOnkoGenetik Kongresi, İskele, Kıbrıs (Kktc), 4 - 07 Mayıs 2023, cilt.1, sa.3308, ss.105

Ailesel Kanser Sendromu Tanısında Göz Ardı Edilmemesi Gereken Bir Gen ‘’Pms1’’: Çanakkale’Den Vaka Serisi

çelik k. m., KAYA D., AKCAN M. B., SILAN F.

15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022

Isolated Colobomatous Microphthalmia Due To A Nonsense Mutation In The Abcb6 Gene: A Rare Case Report

Akcan M. B., Kaya D., Erdoğan H., Sılan F.

15.Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022, ss.269

Importance of genetic diagnosis in demyelinating diseases; adult-onset Alexander Disease case with novel GFAP mutation

CEYLAN KÖSE C., OCAK Ö., GÜNDÜZ O. R., SILAN F.

15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022

Mowat-Wilson Syndrome: A Case Report With Novel Splice Site Mutation In Zeb2 Gene

TEKİN K., AKCAN M. B., KAYA D., SILAN F.

15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022

Konjenital adrenal hiperplazide CYP11B1 homozigot mutasyonu: Vaka sunumu

Kaya D., Tekin K., Karakılıç E., Sılan F.

15. Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022, ss.226

Two Different Pathogenic Mutations In A Patient With Multiple Exostosis And Autism Spectrum Disorder: Case Report With Our Cohort Information

Sönmez V., Ceylan Köse C., Sılan F.

15. Uluslararası Katılımlı Ulusal Tıbbi Genetik Kongresi, Muğla, Türkiye, 9 - 13 Kasım 2022, ss.312

The significance of the BRCA2 c.9934A>G variant is really unknown?A series of patients with BRCA2 c.9934A>G variant among Çanakkale patients

AKCAN M. B., ÇELİK K. M., SILAN F.

EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022

Determination of carrier frequency of SMN1 gene intragenic mutations: Case series

SILAN F., SÖNMEZ V., ÖZTÜRK M.

EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022

A novel BRPF1 variant in a family with intellectual disability and dysmorphic face, from Çanakkale

CEYLAN KÖSE C., KAYA D., AKCAN M. B., SILAN F.

EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022

A patient with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome due to 16p11.2 deletion: a case report from Çanakkale

ÇELİK K. M., ÇAVUŞ E., AKCAN M. B., SILAN F.

EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022

A novel homozygous mutation in CC2D1A gene: two case from a Turkish family in Canakkale

KAYA D., CEYLAN KÖSE C., SILAN F.

EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022

A rare Malpuech, Mignarelli, Michels, Carnevale Syndrome (3MC Syndrome); Novel variant in the MASP1 gene

GÜNDÜZ O. R., CEYLAN KÖSE C., SILAN F.

EUROPEAN BİOTECHNOLOGY CONGRESS 2022, PRAG, Çek Cumhuriyeti, 5 - 07 Ekim 2022

Türkiye NRXN1 intragenik delesyonlarının fenotipik spektrumu: Çanakkale’den bir vaka serisi

ÇELİK K. M., AKCAN M. B., SILAN F.

7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 - 28 Mayıs 2022

22q11.2 duplication syndrome showing clinical variability and overlapping with the features of Digeorge/Velocardiofacial Syndrome: case series from Çanakkale

Akcan M. B., Çelik K. M., Sılan F.

7.Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 Mayıs 2022, ss.161-162

Primary Coenzyme Q10 Deficiency; Determination of Patient and Carrier Frequency in the Çanakkale Cohort

SILAN F., KAYA D., AKBAŞ N. E.

7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 - 28 Mayıs 2022

A rare syndrome from Canakkale; Kindler Syndrome with loss of heterozygosity of FERMT1 gene region

GÜNDÜZ O. R., IŞIK MERMUTLU S., CEYLAN KÖSE C., SILAN F.

7. Uluslararası Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 26 - 28 Mayıs 2022

P-28 Meme Ve Over Kanserinde Kombine Mutasyonlar Tedavi Etkinliğini Değiştirebilir Mi? Ailesinde Meme Ve Over Kanser Öyküsü Olan Vakada Brca1 Ve Sdhb Genleri Patojenik/muhtemel Patojenik Varyant Birlikteliği

CEYLAN KÖSE C., SILAN F., TURAN N. E., SÖNMEZ V., SILAN C.

1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021

Palb2 Genotip Fenotip Korelasyonu: Vaka Serisi

Sönmez V., Akcan M. B., Ecmel Akbaş N., Kaya D., Muge Celik K., Sılan F.

1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1

İzole Pankreas Kanserli Bir Olgunun Ailesinde Saptanan M.patojenik Novel Vhl Mutasyonu Bildirimi

Sönmez V., Kaya D., Akcan M. B., Kablan A., Emre Mutluer Y., Sılan F.

1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1 Sürdürülebilir Kalkınma

Ailevi Kanser Sendromu Ön Tanılı Vakalarda Tp53 Ve Chek2 Genlerinin Analizi: Bir Vaka Serisi

Akcan M. B., Ceylan Köse C., Kaya D., Gündüz O. R., Sönmez V., Sılan F.

1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1 Sürdürülebilir Kalkınma

Geniş Kapsamlı Panel Analizlerinin Klinik Faydası: Ailesinde Yaygın Kanser Öyküsü Olan Pankreas Kanseri Ve Memede Kitle Sebebiyle Takipli Genç Yaş Kadın Hastada Saptanan Chek2 Ve Nbn Patojenik/muhtemel Patojenik Varyantları

Müge Çelik K., Sönmez V., Kaya D., Sılan F.

1. Ulusal HematoOnkoGenetik Kongresi, Antalya, Türkiye, 25 - 28 Kasım 2021, ss.0-1 Sürdürülebilir Kalkınma

The evaluation of FMF course and colchicine treatment in the patients with or without COVID-19 symptoms during the pandemic

Akcan M. B., Albuz B., Sılan F., Özdemir Ö.

6. Uluslararası Katılımlı Erciyes Tıp Tıbbi Genetik Kongresi, Kayseri, Türkiye, 16 - 18 Eylül 2021, ss.0-1 Sürdürülebilir Kalkınma