F. Dincsoy Bir Et Al. , "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," MOLECULAR SYNDROMOLOGY , vol.13, no.3, pp.254-260, 2022
Dincsoy Bir, F. Et Al. 2022. 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. MOLECULAR SYNDROMOLOGY , vol.13, no.3 , 254-260.
Dincsoy Bir, F., SILAN, F., Velickovic, J., Berkay Akcan, M. B., & ÖZDEMİR, Ö., (2022). 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. MOLECULAR SYNDROMOLOGY , vol.13, no.3, 254-260.
Dincsoy Bir, FİRDEVS Et Al. "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," MOLECULAR SYNDROMOLOGY , vol.13, no.3, 254-260, 2022
Dincsoy Bir, FİRDEVS D. Et Al. "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." MOLECULAR SYNDROMOLOGY , vol.13, no.3, pp.254-260, 2022
Dincsoy Bir, F. Et Al. (2022) . "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." MOLECULAR SYNDROMOLOGY , vol.13, no.3, pp.254-260.
@article{article, author={FİRDEVS DİNÇSOY BİR Et Al. }, title={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}, journal={MOLECULAR SYNDROMOLOGY}, year=2022, pages={254-260} }