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Dive into the research topics of 'Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome'. Together they form a unique fingerprint.- Sort by
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Hyung Goo Kim, Ingo Kurth, Fei Lan, Irene Meliciani, Wolfgang Wenzel, Soo Hyun Eom, Gil Bu Kang, Georg Rosenberger, Mustafa Tekin, Metin Ozata, David P. Bick, Richard J. Sherins, Steven L. Walker, Yang Shi, James F. Gusella, Lawrence C Layman
Research output: Contribution to journal › Article › peer-review