Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability-Reference-Cited by-同舟云学术

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Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability

Published:2012-04-09 Issue:2 Volume:83 Page:145-154
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Qiao Y,Tyson C,Hrynchak M,Lopez-Rangel E,Hildebrand J,Martell S,Fawcett C,Kasmara L,Calli K,Harvard C,Liu X,Holden JJA,Lewis SME,Rajcan-Separovic E

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2012.01860.x/fullpdf

Reference12 articles.

1. Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.;Sagoo;Genet Med,2009

2. Functional impact of global rare copy number variation in autism spectrum disorders.;Pinto;Nature,2010

3. Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.;Friedman;BMC Genomics,2009

4. Molecular karyotyping using an SNP array for genomewide genotyping.;Rauch;J Med Genet,2004

5. High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?;Bernardini;Eur J Hum Genet,2010

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