De novo trisomy 16p11.2-qter: Report of an infant
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference7 articles.
1. Trisomy 16q in a female newborn with a de novo X;16 translocation and hypoplastic left heart
2. Partial duplication 16q: report of two affected siblings resulting from a maternal translocation and literature review
3. Molecular studies of non-disjunction in trisomy 16.
4. Partial trisomy 16q in two boys resulting from a maternal translocation, t(15;16) (p12;q11)
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1. Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation;Medicine;2021-02-19
2. Fetal Persistent Left Superior Vena Cava with Trisomy 21: A Case Report and Literature Review;Pediatrics & Neonatology;2016-06
3. Karyotype/phenotype correlation in partial trisomies of the long arm of chromosome 16: Case report and review of literature;American Journal of Medical Genetics Part A;2012-02-21
4. Subtelomeric monosomy 11q and trisomy 16q in siblings and an unrelated child: Molecular characterization of two der(11)t(11;16);American Journal of Medical Genetics Part A;2011-08-10
5. Review of genetic factors in intestinal malrotation;Pediatric Surgery International;2010-06-13
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