Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow-Reference-Cited by-同舟云学术

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Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

Published:2011-06-22 Issue:12 Volume:19 Page:1230-1237
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Srebniak Malgorzata,Boter Marjan,Oudesluijs Grétel,Joosten Marieke,Govaerts Lutgarde,Van Opstal Diane,Galjaard Robert-Jan H

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2011119.pdf

Reference24 articles.

1. Shaffer LG, Coppinger J, Alliman S et al: Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens. Prenat Diagn 2008; 28: 789–795.

2. Rickman L, Fiegler H, Carter NP, Bobrow M : Prenatal diagnosis by array-CGH. Eur J Med Genet 2005; 48: 232–240.

3. Rickman L, Fiegler H, Shaw-Smith C et al: Prenatal detection of unbalanced chromosomal rearrangements by array CGH. J Med Genet 2006; 43: 353–361.

4. Sahoo T, Cheung SW, Ward P et al: Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genet Med 2006; 8: 719–727.

5. Friedman JM : High resolution array genomic hybridization in prenatal diagnosis. Prenat Diagn 2009; 29: 20–28.

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