A case of insertional translocation resulting in partial trisomy 16p
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference20 articles.
1. A familial MCA/MR syndrome due to translocation t(10;16)(q26;p13.1): Report of six cases;Bofinger;Am. J. Med. Genet.,1991
2. Value of chromosome painting in determining the chromosomal outcome in offspring of a 12;16 translocation carrier;Brandt;J. Med. Genet.,1994
3. De novo trisomy 16p;Carrasco;Am. J. Med. Genet.,1997
4. Duplication of 16p from insertion of 16p into 16q with subsequent duplication due to crossing over within the inserted segment;Cohen;Am. J. Med. Genet.,1983
5. De novo’ trisomy 16p11→pter;Dallapicola;Hum. Genet.,1979
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1. De novo 16p13.3-p12.3 duplication in a child with syndromic developmental delay;Gene Reports;2020-09
2. Genotype-phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literature;American Journal of Medical Genetics Part A;2015-12-07
3. Prenatal diagnosis of partial trisomy 16p and its association with congenital diaphragmatic hernia;Prenatal Diagnosis;2013-04-24
4. 16P Subtelomeric Duplication With Vascular Anomalies: An Albanian Case Report And Literature Review;Balkan Journal of Medical Genetics;2012-12-01
5. Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization;Taiwanese Journal of Obstetrics and Gynecology;2010-12
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