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1998•Journal of the Society for Gynecologic InvestigationRequires access

The low frequency of Kallmann syndrome (KAL) gene mutations in humans with hypogonadotropic hypogonadism suggests non-x linked modes of inheritance

Lawrence Clarke Layman, E KALIMULLAH, G. Boachie‐Ansah, Jun Hua Xie, M JIN, Sewit Amde, Sudeep R. Shah, Patricia S. Kawada, W PARNPOONSUP, Richard J. Sherins

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Key concepts: Kallmann syndrome, Hypogonadotropic hypogonadism, Inheritance (genetic algorithm), Genetics, Gene, Mutation, Internal medicine, Medicine

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The low frequency of Kallmann syndrome (KAL) gene mutations in humans with hypogonadotropic hypogonadism suggests non-x linked modes of inheritance — Research Paper | ScholarLens