Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann SyndromeHyung‐Goo Kim, Lawrence C. Layman, Wolfgang Wenzel et al.|The American Journal of Human Genetics|2008Cited by 332
WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann SyndromeHyung‐Goo Kim, Lawrence C. Layman, Jang-Won Ahn et al.|The American Journal of Human Genetics|2010Cited by 195