Prenatal diagnosis of trisomy 6q25.3‐qter and monosomy 10q26.12‐qter by array CGH in a fetus with an apparently normal karyotype-Reference-Cited by-同舟云学术

Prenatal diagnosis of trisomy 6q25.3‐qter and monosomy 10q26.12‐qter by array CGH in a fetus with an apparently normal karyotype

Published:2014-10-15 Issue:2 Volume:3 Page:92-95
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Marinescu Ponnila S.¹,Saller Devereux N.²,Parks W. Tony³,Yatsenko Svetlana A.²³,Rajkovic Aleksandar²³⁴

Affiliation:

1. Department of Obstetrics and Gynecology University of Virginia Health System Charlottesville Virginia

2. Division of Medical Genetics Department of Obstetrics Gynecology and Reproductive Sciences Magee‐Womens Hospital of University of Pittsburgh Medical Center Pittsburgh Pennsylvania

3. Department of Pathology University of Pittsburgh School of Medicine Pittsburgh Pennsylvania

4. Department of Human Genetics University of Pittsburgh School of Medicine Pittsburgh Pennsylvania

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.162

Reference12 articles.

1. Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation;Grouchy J.;Ann. Genet.,1969

2. Dysmorphic sibs trisomic for the region 6q22.1right-arrow6q23.3

3. Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome.

4. Prenatal diagnosis of a de novo trisomy 6q22.2→6qter and monosomy lpter→1p36.3. Case report with a 2-year follow-up and a brief review of other prenatal cases of partial trisomy 6q

5. Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases

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