22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference37 articles.
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1. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother;Taiwanese Journal of Obstetrics and Gynecology;2021-01
2. El síndrome 22q11.2DS como un subtipo genético de esquizofrenia;Revista Colombiana de Psiquiatría;2015-01
3. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family;Taiwanese Journal of Obstetrics and Gynecology;2013-12
4. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review;Gene;2013-09
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