Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH-Reference-Cited by-同舟云学术

Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH

Published:2006-08 Issue:2 Volume:88 Page:152-162
ISSN:0888-7543
Container-title:Genomics
language:en
Short-container-title:Genomics

Author:

de Bustos Cecilia,Díaz de Ståhl Teresita,Piotrowski Arkadiusz,Mantripragada Kiran K.,Buckley Patrick G.,Darai Eva,Hansson Caisa M.,Grigelionis Gintautas,Menzel Uwe,Dumanski Jan P.

Publisher

Elsevier BV

Subject

Genetics

Reference54 articles.

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3. DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets;Mantripragada;Int. J. Mol. Med.,2004

4. Copy-number polymorphisms: mining the tip of an iceberg;Buckley;Trends Genet.,2005

5. Detection of large-scale variation in the human genome;Iafrate;Nat. Genet.,2004

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1. Genome-Wide Identification of Copy Number Variations in Chinese Holstein;PLoS ONE;2012-11-07

2. Comparative Genomic Hybridization to Detect Variation in the Copy Number of Large DNA Segments;Cold Spring Harbor Protocols;2011-11

3. Copy number variation in African Americans;BMC Genetics;2009-03-24

4. Unambiguous molecular detections with multiple genetic approach for the complicated chromosome 22q11 deletion syndrome;BMC Medical Genetics;2009-02-25

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