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Fraser syndrome due to mutations in GRIP1 —Clinical phenotype in two families and expansion of the mutation spectrum
Author(s) -
Schanze Denny,
Kayserili Hülya,
Satkın Bilge N.,
Altunoglu Umut,
Zenker Martin
Publication year - 2014
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.36343
Subject(s) - medical genetics , university hospital , medical school , human genetics , medicine , genetics , family medicine , medical education , biology , gene
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