Metin Özata

1 ta ish

GATA Haydarpaşa Eğitim Hastanesi

1. Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

   Hyung‐Goo Kim, Ingo Kurth, Fei Lan +13

   Maqola20082 iqtibos

   ABIABI:AkademIndex/2026.other.720842