A novel mutation of AMHR2 in two siblings with persistent Müllerian duct syndrome
Makaleler > Tam Makale · 2018
Yazarlar: Edip Unal, Yusuf Kenan Haspolat, Ruken Yıldırım, Suat Tekin, Vasfiye Demir, Hüseyin Onay
Journal of Clinical Research in Pediatric Endocrinology, Uluslararası, Wos, 2018, cilt 10, ss 387-390
DOI: 10.4274/jcrpe.0013
Özet
gene that was identified for the first time. This presented with different phenotypes in two siblings.