Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20-Reference-Cited by-同舟云学术

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Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20

Published:2009-08-10 Issue:10 Volume:29 Page:1002-1005
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Callier P.,Faivre L.,Pigeonnat S.,Quilichini B.,Marle N.,Thauvin-Robinet C.,Mosca A. L.,Masurel-Paulet A.,Rousseau T.,Sagot P.,Laurent N.,Mugneret F.

Funder

Direction de la Recherche Clinique du CHU de Dijon

Conseil Regional de Bourgogne “2008”

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.2333/fullpdf

Reference12 articles.

1. Mechanisms and consequences of small supernumerary marker chromosomes: from Barbara McClintock to modern genetic-counseling issues;Baldwin;Am J Hum Genet,2008

2. Detection of low-level mosaicism by array CGH in routine diagnostic specimens;Ballif;Am J Med Genet A,2006

3. Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formation;Bartels;Cytogenet Genome Res,2003

4. An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line;Batista;Prenat Diagn,1995

5. Prenatal diagnosis of minute supernumerary marker chromosomes;Cotter;Gynecol Obstet Invest,2005

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Clinical Observation of a Child with Prenatally Diagnosed De Novo Partial Trisomy of Chromosome 20;Fetal and Pediatric Pathology;2019-03-20

2. Chromosomal Abnormalities in Preimplantation Embryos and Detection Strategies in PGD and PGS;Chromosomal Abnormalities - A Hallmark Manifestation of Genomic Instability;2017-08-30

3. An Improved Method to Extract DNA from 1 ml of Uncultured Amniotic Fluid from Patients at Less than 16 Weeks’ Gestation;PLoS ONE;2013-04-02

4. A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity;Genetics in Medicine;2013-01

5. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59Mb in 10p15.3–p14 and 4.22Mb in 10q26.3;European Journal of Medical Genetics;2012-01

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