Partial Trisomy 10q (10q25.1 →qter) and Partial Monosomy 13q (13q34→qter) Presenting With Fetal Pyelectasis: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization-Reference-Cited by-同舟云学术

Partial Trisomy 10q (10q25.1 →qter) and Partial Monosomy 13q (13q34→qter) Presenting With Fetal Pyelectasis: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization

Published:2010-12 Issue:4 Volume:49 Page:539-543
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Su Yi-Ning,Tsai Fuu-Jen,Chern Schu-Rern,Hsu Chin-Yuan,Wu Pei-Chen,Lee Chen-Chi,Chen Wen-Lin,Wang Wayseen

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

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2. New chromosomal syndromes. I. Partial trisomy of the distal portion of the long arm of chromosome number 10 (10q24→qter): a clinical entity;Fryns;Acta Paediatr Belg,1979

3. Partial trisomy 10q, a recognizable syndrome;Klep-de Pater;Hum Genet,1979

4. Chromosome 10, trisomy 10q2;Fryns,1990

5. 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);García-Heras;J Med Genet,1997

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1. A rare unbalanced translocation (trisomy 5q33.3‐qter, monosomy 13q34‐qter) results in growth hormone deficiency and brain anomalies;Molecular Genetics & Genomic Medicine;2021-10-08

2. 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

3. Prenatal diagnosis of sub-microscopic partial trisomy 10q using chromosomal microarray analysis in a phenotypically abnormal fetus with normal karyotype;Journal of Neonatal-Perinatal Medicine;2016-06-22

4. Unbalanced Translocations Involving Chromosome Region 10q25.3q26.3 in Patients with Intellectual Disability and Complex Phenotypes;Cytogenetic and Genome Research;2014

5. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13;Gene;2013-10