Autor/in Kim, Hyung-Goo 2 Kurth, Ingo Lan, Fei Bick, David P 1 Eom, Soo Hyun 1 Kang, Gil Bu 1 Kim, Hyun-Taek 1 Leach, Natalia T 1 Meliciani, Irene 1 Nowka, Anna 1 Ozata, Metin 1 Rosenberger, Georg 1 Seong, Ihn Sik 1 Shen, Yiping 1 Silahtaroglu, Asli 1 Talkowski, Michael E 1 Tekin, Mustafa 1 Ullmann, Reinhard 1 Wenzel, Wolfgang 1 alle zeigenListe einklappen
Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies. Kim, Hyung-Goo Kim, Hyun-Taek Leach, Natalia T Lan, Fei Ullmann, Reinhard Silahtaroglu, Asli Kurth, Ingo 2012 - Forschungsinformationssystem des UKE
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
