Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1?qter)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference5 articles.
1. Fetal pyelectasis in consecutive pregnancies: a possible genetic predisposition
2. 1990. Chromosome 10, trisomy 10q2. In Birth Defects Encyclopedia, (ed). Blackwell Scientific Publications: Cambridge; 359-360.
3. De novo der(X)t(X;10)(q26;q21) with features of distal trisomy 10q: case report of paternal origin identified by late replication with BrdU and the human androgen receptor assay (HAR).
4. Fetal pyelectasis
5. Antenatal Diagnosis of Upper Urinary Tract Dilation by Ultrasonography
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1. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results;Taiwanese Journal of Obstetrics and Gynecology;2020-09
2. Unbalanced reciprocal translocations at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2011-03
3. Partial Trisomy 10q (10q25.1 →qter) and Partial Monosomy 13q (13q34→qter) Presenting With Fetal Pyelectasis: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization;Taiwanese Journal of Obstetrics and Gynecology;2010-12
4. NFκB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 → qter);Prenatal Diagnosis;2008
5. Extraction and evaluation of urban agriculture region based on RS and GIS: a case study in Beijing;SPIE Proceedings;2007-06-10
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