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

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

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

Oxford University Press

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Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: Case Report

By Juul A.   Aksglaede L.   Lund A.M.   Duno M.   Skakkebk N.E.   Rajpert-De Meyts E.  

Human Reproduction, Vol. 22, Iss. 7, 2007-07 ,pp. : 1907-1911

Oxford University Press

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Homozygous mutation in the prokineticin-receptor2 gene (Val274Asp) presenting as reversible Kallmann syndrome and persistent oligozoospermia: Case Report

By Sinisi Antonio Agostino   Asci Roberta   Bellastella Giuseppe   Maione Luigi   Esposito Dario   Elefante Andrea   De Bellis Annamaria   Bellastella Antonio   Iolascon Achille  

Human Reproduction, Vol. 23, Iss. 10, 2008-10 ,pp. : 2380-2384

Oxford University Press

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Fibroblast Growth Factor Receptor 1 as a Putative Therapy Target in Colorectal Cancer

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Digestion, Vol. 88, Iss. 3, 2013-10 ,pp. : 172-181

Karger

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Case report. High dose gonadotrophin-releasing hormone antagonist (ganirelix) may prevent ovarian hyperstimulation syndrome caused by ovarian stimulation for in-vitro fertilization

By de Jong D  

Human Reproduction, Vol. 13, Iss. 3, 1998-03 ,pp. : 573-575

Oxford University Press

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