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
Cumhuriyet Tıp Dergisi (ELEKTRONİK), vol.44, no.1, pp.125-130, 2022 (Peer-Reviewed Journal)
- Publication Type: Article / Case Report
- Volume: 44 Issue: 1
- Publication Date: 2022
- Doi Number: 10.7197/cmj.989474
- Journal Name: Cumhuriyet Tıp Dergisi (ELEKTRONİK)
- Journal Indexes: Index Copernicus
- Page Numbers: pp.125-130
- Open Archive Collection: AVESIS Open Access Collection
- Çanakkale Onsekiz Mart University Affiliated: Yes