Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference33 articles.
1. A familial MCA/MR syndrome due to translocation t(10;16)(q26;p13.1): Report of six cases
2. del(15)(q22q24) Syndrome with Potter sequence
3. Alternate, adjacent 2 and 3:1 meiotic segregation products from a balanced t(13;18) (q12;q11) carrier
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2. Etiology and management of early pregnancy renal anhydramnios: Is there a place for serial amnioinfusions?;Prenatal Diagnosis;2020-02-19
3. Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester;Taiwanese Journal of Obstetrics and Gynecology;2012-03
4. Unbalanced translocation 9;16 in two children with dysmorphic features, and severe developmental delay: Evidence of cross-over within derivative chromosome 9 in patient #1;European Journal of Medical Genetics;2011-03
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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