Kallmann Syndrome Due to a Novel<i>FGFR1</i>Gene Mutation

Flint, Amanda; Witchel, Selma F.; Chemaitilly, Wassim

doi:10.1210/endo-meetings.2011.part1.or6.or05-3

TRANSLATIONAL - Genetics &Amp; Epigenetics in GnRH Regulation 2011

DOI: 10.1210/endo-meetings.2011.part1.or6.or05-3

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Kallmann Syndrome Due to a NovelFGFR1Gene Mutation

Amanda Flint¹,

Selma F. Witchel²,

Wassim Chemaitilly³

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Kallmann Syndrome Due to a NovelFGFR1Gene Mutation

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