Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations
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Published:2015-08
Issue:8
Volume:17
Page:651-659
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ISSN:1098-3600
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Container-title:Genetics in Medicine
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language:en
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Short-container-title:Genetics in Medicine
Author:
Villanueva CarineORCID,
Jacobson-Dickman Elka,
Xu Cheng,
Manouvrier Sylvie,
Dwyer Andrew A.,
Sykiotis Gerasimos P.,
Beenken Andrew,
Liu Yang,
Tommiska Johanna,
Hu Youli,
Tiosano Dov,
Gerard Marion,
Leger Juliane,
Drouin-Garraud Valérie,
Lefebvre Hervé,
Polak Michel,
Carel Jean-Claude,
Phan-Hug Franziska,
Hauschild MichaelORCID,
Plummer Lacey,
Rey Jean-Pierre,
Raivio TaneliORCID,
Bouloux Pierre,
Sidis Yisrael,
Mohammadi MoosaORCID,
de Roux Nicolas,
Pitteloud Nelly
Subject
Genetics (clinical)
Cited by
56 articles.
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