Javad Mohammadi asl
۴ مقاله۲ نشریهسالهای فعالیت: ۲۰۱۶–۲۰۲۱
- Ahvaz Jundishapour University of Medical Sciences, Ahvaz, Iran. (۲۰۱۶–۲۰۲۱)
20162021
مقالهها (۴)
Utilization of Whole Exome Sequencing in Non-Syndromic Premature Ovarian Failure: Ficolin-3 Gene Mutation in an Iranian Family
Identification of a Novel Stop Loss Mutation in P2RX2 Gene in an Iranian Family with Autosomal Nonsyndromic Hearing Loss
Next-Generation Sequencing Reveals One Novel Missense Mutation in COL1A2 Gene in an Iranian Family with Osteogenesis imperfecta
A Novel Splicesite Mutation in the EDAR Gene Causes Severe Autosomal Recessive Hypohydrotic (Anhidrotic) Ectodermal Dysplasia in an Iranian Family