Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities-Reference-Cited by-同舟云学术

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities

Published:2012 Issue:1 Volume:5 Page:14
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Srebniak Malgorzata I,Boter Marjan,Oudesluijs Gretel O,Cohen-Overbeek Titia,Govaerts Lutgarde CP,Diderich Karin EM,Oegema Renske,Knapen Maarten FCM,van de Laar Ingrid MBH,Joosten Marieke,Van Opstal Diane,Galjaard Robert-Jan H

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry, medical,Genetics(clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Reference8 articles.

1. Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

2. Visualization of Shared Genomic Regions and Meiotic Recombination in High-Density SNP Data

3. Outcome of cases ofde novo structural rearrangements diagnosed at amniocentesis

4. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

5. High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings

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