Loading…

Macrothrombocytopenia as diagnosis predictor of 22q11 deletion syndrome among patients with congenital heart defects

Saved in:

Bibliographic Details
Published in:	American journal of medical genetics. Part A 2015-06, Vol.167A (6), p.1406-1408
Main Authors:	Trevisan, Patrícia, Barbosa, Sílvia, Sperotto, Graziela, Costi, Caroline, de Omena Filho, Reinaldo L., Silva, Alessandra P. da, Varella-Garcia, Marileila, Fiegenbaum, Marilu, Rosa, Rafael F. M., Zen, Paulo R. G.
Format:	Article
Language:	English
Subjects:	22q11 Deletion Syndrome - diagnosis 22q11 Deletion Syndrome - genetics 22q11 Deletion Syndrome - pathology Biomarkers - analysis Female Heart Defects, Congenital - diagnosis Heart Defects, Congenital - genetics Heart Defects, Congenital - pathology Humans In Situ Hybridization, Fluorescence Infant Karyotyping Male Predictive Value of Tests Prospective Studies ROC Curve Thrombocytopenia - diagnosis Thrombocytopenia - genetics Thrombocytopenia - pathology
Citations:	Items that this one cites Items that cite this one
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!