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Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.

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Title: Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
Authors: Pitteloud N; Reproductive Endocrine Unit of the Department of Medicine and Harvard Reproductive Endocrine Science Centers, Massachusetts General Hospital, 55 Fruit Street, Boston, MA 02114, USA. npitteloud@partners.org, Acierno JS Jr, Meysing A, Eliseenkova AV, Ma J, Ibrahimi OA, Metzger DL, Hayes FJ, Dwyer AA, Hughes VA, Yialamas M, Hall JE, Grant E, Mohammadi M, Crowley WF Jr
Source: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2006 Apr 18; Vol. 103 (16), pp. 6281-6. Date of Electronic Publication: 2006 Apr 10.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0027-8424 (Print) Linking ISSN: 00278424 NLM ISO Abbreviation: Proc Natl Acad Sci U S A Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
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  Data: Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
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  Data: <searchLink fieldCode="AU" term="%22Pitteloud+N%22">Pitteloud N</searchLink>; Reproductive Endocrine Unit of the Department of Medicine and Harvard Reproductive Endocrine Science Centers, Massachusetts General Hospital, 55 Fruit Street, Boston, MA 02114, USA. npitteloud@partners.org<br /><searchLink fieldCode="AU" term="%22Acierno+JS+Jr%22">Acierno JS Jr</searchLink><br /><searchLink fieldCode="AU" term="%22Meysing+A%22">Meysing A</searchLink><br /><searchLink fieldCode="AU" term="%22Eliseenkova+AV%22">Eliseenkova AV</searchLink><br /><searchLink fieldCode="AU" term="%22Ma+J%22">Ma J</searchLink><br /><searchLink fieldCode="AU" term="%22Ibrahimi+OA%22">Ibrahimi OA</searchLink><br /><searchLink fieldCode="AU" term="%22Metzger+DL%22">Metzger DL</searchLink><br /><searchLink fieldCode="AU" term="%22Hayes+FJ%22">Hayes FJ</searchLink><br /><searchLink fieldCode="AU" term="%22Dwyer+AA%22">Dwyer AA</searchLink><br /><searchLink fieldCode="AU" term="%22Hughes+VA%22">Hughes VA</searchLink><br /><searchLink fieldCode="AU" term="%22Yialamas+M%22">Yialamas M</searchLink><br /><searchLink fieldCode="AU" term="%22Hall+JE%22">Hall JE</searchLink><br /><searchLink fieldCode="AU" term="%22Grant+E%22">Grant E</searchLink><br /><searchLink fieldCode="AU" term="%22Mohammadi+M%22">Mohammadi M</searchLink><br /><searchLink fieldCode="AU" term="%22Crowley+WF+Jr%22">Crowley WF Jr</searchLink>
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  Data: <searchLink fieldCode="JN" term="%227505876%22">Proceedings of the National Academy of Sciences of the United States of America</searchLink> [Proc Natl Acad Sci U S A] 2006 Apr 18; Vol. 103 (16), pp. 6281-6. <i>Date of Electronic Publication: </i>2006 Apr 10.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22National+Academy+of+Sciences%22">National Academy of Sciences </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>7505876 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0027-8424 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200278424%22">00278424 </searchLink><i>NLM ISO Abbreviation: </i>Proc Natl Acad Sci U S A <i>Subsets: </i>MEDLINE
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        Value: 10.1073/pnas.0600962103
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      – Code: eng
        Text: English
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        StartPage: 6281
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      – TitleFull: Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.
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              Text: 2006 Apr 18
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