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Concurrent diagnoses of Prader–Willi syndrome and GM2 gangliosidosis caused by uniparental disomy of chromosome 15
Author(s) -
Regier Debra S.,
Leon Eyby,
Counts Debra R.,
Tifft Cynthia J.,
Zand Dina J.
Publication year - 2015
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.37090
Subject(s) - medical genetics , uniparental disomy , library science , family medicine , medicine , gerontology , genetics , biology , chromosome , gene , computer science , karyotype
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