Low-level mosaicism of trisomy 14: Phenotypic and molecular characterization-Reference-Cited by-同舟云学术

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Low-level mosaicism of trisomy 14: Phenotypic and molecular characterization

Published:2008 Issue:11 Volume:146A Page:1395-1405
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shinawi Marwan,Shao Lina,Jeng Linda Jo Bone,Shaw Chad A.,Patel Ankita,Bacino Carlos,Sutton Vernon R.,Belmont John,Cheung Sau Wai

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference31 articles.

1. Detection of low-level mosaicism by array CGH in routine diagnostic specimens

2. Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH

3. Development and validation of a CGH microarray for clinical cytogenetic diagnosis

4. Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

5. Natural history of mosaic trisomy 14 syndrome

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1. High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with congenital heart defects and intrauterine growth restriction on fetal ultrasound;Taiwanese Journal of Obstetrics and Gynecology;2023-07

2. A Rare Combination of Chromosomal Abnormalities in an Infant With Turner Syndrome and Hypoplastic Left Heart Syndrome;Cureus;2021-07-20

3. Sequencing approaches;Cytogenomics;2021

4. Low-Level Trisomy 14 Mosaicism: A Carrier of an Isochromosome 14 and a Supernumerary Marker Chromosome 14;Cytogenetic and Genome Research;2020

5. Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation;Cytogenetic and Genome Research;2020

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