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Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.

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Title: Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
Authors: Pitteloud N; Reproductive Endocrine Unit of the Department of Medicine & National Center for Infertility Research, Bartlett Hall Extension 5, Massachusetts General Hospital, 55 Fruit St., Boston, MA 02114, United States. npitteloud@partners.org, Meysing A, Quinton R, Acierno JS Jr, Dwyer AA, Plummer L, Fliers E, Boepple P, Hayes F, Seminara S, Hughes VA, Ma J, Bouloux P, Mohammadi M, Crowley WF Jr
Source: Molecular and cellular endocrinology [Mol Cell Endocrinol] 2006 Jul 25; Vol. 254-255, pp. 60-9. Date of Electronic Publication: 2006 Jun 09.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: North Holland Publishing Country of Publication: Ireland NLM ID: 7500844 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0303-7207 (Print) Linking ISSN: 03037207 NLM ISO Abbreviation: Mol Cell Endocrinol Subsets: MEDLINE
Database: MEDLINE Ultimate
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An: 16764984
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
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  Data: <searchLink fieldCode="AU" term="%22Pitteloud+N%22">Pitteloud N</searchLink>; Reproductive Endocrine Unit of the Department of Medicine & National Center for Infertility Research, Bartlett Hall Extension 5, Massachusetts General Hospital, 55 Fruit St., Boston, MA 02114, United States. npitteloud@partners.org<br /><searchLink fieldCode="AU" term="%22Meysing+A%22">Meysing A</searchLink><br /><searchLink fieldCode="AU" term="%22Quinton+R%22">Quinton R</searchLink><br /><searchLink fieldCode="AU" term="%22Acierno+JS+Jr%22">Acierno JS Jr</searchLink><br /><searchLink fieldCode="AU" term="%22Dwyer+AA%22">Dwyer AA</searchLink><br /><searchLink fieldCode="AU" term="%22Plummer+L%22">Plummer L</searchLink><br /><searchLink fieldCode="AU" term="%22Fliers+E%22">Fliers E</searchLink><br /><searchLink fieldCode="AU" term="%22Boepple+P%22">Boepple P</searchLink><br /><searchLink fieldCode="AU" term="%22Hayes+F%22">Hayes F</searchLink><br /><searchLink fieldCode="AU" term="%22Seminara+S%22">Seminara S</searchLink><br /><searchLink fieldCode="AU" term="%22Hughes+VA%22">Hughes VA</searchLink><br /><searchLink fieldCode="AU" term="%22Ma+J%22">Ma J</searchLink><br /><searchLink fieldCode="AU" term="%22Bouloux+P%22">Bouloux P</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="%227500844%22">Molecular and cellular endocrinology</searchLink> [Mol Cell Endocrinol] 2006 Jul 25; Vol. 254-255, pp. 60-9. <i>Date of Electronic Publication: </i>2006 Jun 09.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22North+Holland+Publishing%22">North Holland Publishing </searchLink><i>Country of Publication: </i>Ireland <i>NLM ID: </i>7500844 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Print <i>ISSN: </i>0303-7207 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2203037207%22">03037207 </searchLink><i>NLM ISO Abbreviation: </i>Mol Cell Endocrinol <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1016/j.mce.2006.04.021
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      – Code: eng
        Text: English
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        StartPage: 60
    Titles:
      – TitleFull: Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.
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            – D: 25
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              Text: 2006 Jul 25
              Type: published
              Y: 2006
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              Value: 254-255
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            – TitleFull: Molecular and cellular endocrinology
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