Publications & Works

Publication Network

Published journal articles indexed by SCI, SSCI, and AHCI

First note on marine-like cementation of Late Holocene beachrock, Iznik Lake (Turkey)

ERGİNAL A. E., Kiyak N. G., ÖZTÜRK M., Yiğitbaş E., Bozcu M., Avcıoğlu M., et al.
GEOCHRONOMETRIA, vol.39, no.1, pp.76-83, 2012 (SCI-Expanded) Sustainable Development identifier identifier

Articles Published in Other Journals

Amyand's hernia detected incidentally in two patients

Resorlu M., Aylanç N., KARATAĞ O., ÖZTÜRK M.
BMJ Case Reports, vol.2017, 2017 (Scopus) identifier identifier

Refereed Congress / Symposium Publications in Proceedings

BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q

ALBUZ B., SILAN F., ÖZTÜRK M., YILDIZ O., ÖZDEMİR Ö.
13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.22, pp.156-1156

A rare heterochromatin polymorphism of chromosome 6 associated with recurrent miscarriage: A case report

ALBUZ B., SILAN F., ÖZTÜRK M., KARAKAYA T., ÖZDEMİR Ö.
13.Balkan Congress of Human Genetics, Edirne, Turkey, 17 - 20 April 2019, vol.0

Fetus with partial trisomy 4 and t(216) due to maternal complex rearrangement involving three chromosomes: a case report

ALBUZ B., ÇETİN G. O., ÖZTÜRK M., CANER V., SEMERCİ GÜNDÜZ C. N., BAĞCI G.
European Human Genetics Conference 2018, 16 - 19 June 2018

A novel nonsense mutation in the EYA1 gene found in a patient with BOR syndrome

ÖZTÜRK M., ZEYBEK S., DURSUN B., ALBUZ B., BOZ Ö., GÜRKAN H., et al.
European Human Genetics Conference 2018, 16 - 19 June 2018

Further delineation of ACPHD syndrome and a novel mutation in DNAJC3

ZEYBEK S., Farre G., ÖZTÜRK M., ALBUZ B., Beltran S., Bowcock A., et al.
European Human Genetics Conference 2018, 16 - 19 June 2018

The co-existence of Nablus Mask-Like Syndrome and Klinefelter Syndrome

BOZ Ö., SARIKEPE B., ZEYBEK S., ÖZTÜRK M., BAĞCI G., ÇETİN G. O.
European Human Genetics Conference 2018, 16 - 19 June 2018

The co-existence of Nablus mask-like facial syndrome and klinefelter syndrome

BOZ Ö., SARIKEPE B., ZEYBEK S., ÖZTÜRK M., BAĞCI G., ÇETİN G. O.
Erciyes Tıp Genetik Günleri 2018, Kayseri, Turkey, 7 - 10 March 2018, vol.40, pp.71

fetus with partial trisomy 4 and t (216) due to maternal complex rearragement involving three chromosome: a case report

ALBUZ B., ÇETİN G. O., ÖZTÜRK M., CANER V., SEMERCİ GÜNDÜZ C. N., BAĞCI G.
ERCİYES MEDİCAL GENETİCS DAYS 1017, Kayseri, Turkey, 11 - 13 May 2017

unbalanced chromosomal rearrangement in fetus with congenital anomaly:a case report

ÖZTÜRK M., ÇETİN G. O., ALBUZ B., CANER V., SEMERCİ GÜNDÜZ C. N., BAĞCI G.
ERCİYES MEDİCAL GENETİCS DAYS 2017, Kayseri, Turkey, 11 - 13 May 2017

A case with vascular anomalies: Differential diagnosis and management

ALBUZ B., KOCAMAZ H., ÖZTÜRK M., SARIKEPE B., TEPELİ E., BAĞCI G., et al.
ERCİYES MEDİCAL GENETİCS DAYS 2017, Kayseri, Turkey, 11 - 13 May 2017

Books & Book Chapters

OTOİNFLAMATUAR HASTALIKLAR VE GENETİK

ÖZTÜRK M., ALBUZ B., SILAN F.
in: Türkiye Klinikleri Tıbbi Genetik - Özel Konular Genetik ve Multidisipliner Yaklaşımlar, Prof Dr C. Nur SEMERCİ GÜNDÜZ, Editor, http://www.turkiyeklinikleri.com, Ankara, pp.49-61, 2019