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Macrothrombocytopenia as diagnosis predictor of 22q11 deletion syndrome among patients with congenital heart defects
Author(s) -
Trevisan Patrícia,
Barbosa Sílvia,
Sperotto Graziela,
Costi Caroline,
de Omena Filho Reinaldo L.,
Silva Alessandra P. da,
VarellaGarcia Marileila,
Fiegenbaum Marilu,
Rosa Rafael F. M.,
Zen Paulo R. G.
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.36531
Subject(s) - deletion syndrome , medicine , cardiology , pediatrics , genetics , biology , phenotype , gene