Autor/in Kim, Hyung-Goo Kurth, Ingo Kim, Hyun-Taek 2 Lan, Fei 2 Meliciani, Irene 2 Ullmann, Reinhard 2 Wenzel, Wolfgang 2 Ahn, Jang-Won 1 Bick, David P 1 Eom, Soo Hyun 1 Ha, Kyung-Soo 1 Itokawa, Yasuhide 1 Kang, Gil Bu 1 Kulharya, Anita 1 Leach, Natalia T 1 Lee, Deresa 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 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
WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome. Kim, Hyung-Goo Ahn, Jang-Won Kurth, Ingo Ullmann, Reinhard Kim, Hyun-Taek Kulharya, Anita Ha, Kyung-Soo 2010 - 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
