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Isolated hypermethylation of GRB10 (7p12.2) in a Silver–Russell syndrome patient carrying a 20p13 microdeletion
Author(s) -
Eggermann T.,
SchneiderRätzke B.,
Begemann M.,
Spengler S.
Publication year - 2014
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/cge.12186
Subject(s) - library science , medicine , genetics , biology , computer science