Autor/in Bick, David P 1 Eom, Soo Hyun 1 Kang, Gil Bu 1 Kim, Hyung-Goo 1 Kurth, Ingo 1 Lan, Fei 1 Meliciani, Irene 1 Ozata, Metin 1 Rosenberger, Georg 1 Tekin, Mustafa Wenzel, Wolfgang alle zeigenListe einklappen
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Kim, Hyung-Goo Kurth, Ingo Lan, Fei Meliciani, Irene Wenzel, Wolfgang Eom, Soo Hyun Kang, Gil Bu 2008 - Forschungsinformationssystem des UKE
