Autor/in Kim, Hyun-Taek 2 Kim, Hyung-Goo 2 Kurth, Ingo 2 Ullmann, Reinhard Ahn, Jang-Won 1 Ha, Kyung-Soo 1 Itokawa, Yasuhide 1 Kulharya, Anita 1 Lan, Fei 1 Leach, Natalia T 1 Lee, Deresa 1 Meliciani, Irene 1 Nowka, Anna 1 Seong, Ihn Sik 1 Shen, Yiping 1 Silahtaroglu, Asli 1 Talkowski, Michael E 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
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
