Autori: Dincsoy Bir Firdevs
| Naslov | 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 (Article) |
| Autori | Dincsoy Bir Firdevs Silan Fatma Velickovic Jelena  Berkay Akcan Mehmet Ozdemir Ozturk
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| Info | MOLECULAR SYNDROMOLOGY, (2022), vol. 13 br. 3, str. 254-260 |
| Projekat | Scientific Research Foundation Unit (BAP) of Canakkale Onsekiz Mart University, Canakkale-Turkey [BAP-TAY2015/445] |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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