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Genetic modifier to chromatin may contribute to 22q11 deletion/VCF/DiGeorge syndrome variability
Author(s) -
Deborah Levenson
Publication year - 2012
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.35798
Subject(s) - digeorge syndrome , chromatin , genetics , gene , biology , genetic disorder , medicine
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