Array CGH in molecular diagnosis of mental retardation-A study of 150 Finnish patients-Reference-Cited by-同舟云学术

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Array CGH in molecular diagnosis of mental retardation-A study of 150 Finnish patients

Published:2010 Issue: Volume: Page:n/a-n/a
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Siggberg Linda,Ala-Mello Sirpa,Jaakkola Elisa,Kuusinen Esa,Schuit Robert,Kohlhase Jürgen,Böhm Detlef,Ignatius Jaakko,Knuutila Sakari

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33402/fullpdf

Reference62 articles.

1. Duplication 9q34 syndrome;Allderdice;Am J Hum Genet,1983

2. Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features;Aradhya;Am J Med Genet Part A,2007

3. Recurrent 10q22-q23 deletions: A genomic disorder on 10q associated with cognitive and behavioral abnormalities;Balciuniene;Am J Hum Genet,2007

4. Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data;Baross;BMC Bioinformatics,2007

5. Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene;Bedeschi;Am J Med Genet Part A,2008

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