A case of Kallmann syndrome carrying a missense mutation in alternatively spliced exon 8A encoding the immunoglobulin-like domain IIIb of fibroblast growth factor receptor 1

Author： Miura Kiyonori   Miura Shoko   Yoshiura Koh-ichiro   Seminara Stephanie   Hamaguchi Daisuke   Niikawa Norio   Masuzaki Hideaki  

Publisher： Oxford University Press

ISSN： 1460-2350

Source： Human Reproduction, Vol.25, Iss.4, 2010-04, pp. : 1076-1080

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