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Congenital hypogonadotropic hypogonadism with anosmia and Gorlin features caused by a PTCH1 mutation reveals a new candidate gene for Kallmann syndrome (vol 111, pg 99, 2020)

S. Barraud,B. Delemer, C. Poirsier-Violle,J. Bouligand, J-J Merol, F. Grange,B. Higel-Chaufour,B. Decoudier,M. Zalzali,A. A. Dwyer,J. S. Acierno,N. Pitteloud,R. P. Millar, J. Young

NEUROENDOCRINOLOGY（2020）

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