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The Journal of Clinical Endocrinology and Metabolism|April 12, 2001
Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadismM Beranova, L M Oliveira, G Y Bédécarrats, et al.Clinical Genetics|November 22, 2008
CHD7 mutations in patients initially diagnosed with Kallmann syndrome--the clinical overlap with CHARGE syndromeM C J Jongmans, C M A van Ravenswaaij-Arts, N Pitteloud, et al.Pageof 2