Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference10 articles.
1. Trisomy 16q in a female newborn with a de novo X;16 translocation and hypoplastic left heart
2. 1990. Chromosome 16, trisomy 16q. In British Defects Encyclopedia, (ed.). Blackwell Scientific Publications: Cambridge; 278-280.
3. Trisomy 16 fetus surviving into the second trimester
4. Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis.
5. De novo trisomy 16p11.2-qter: Report of an infant
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1. A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature;American Journal of Medical Genetics Part A;2021-06
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3. Recurrent Distal 16q Duplication and Terminal 22q Deletion: Prenatal Diagnosis and Genetic Counseling;Taiwanese Journal of Obstetrics and Gynecology;2010-12
4. 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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