Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities-Reference-Cited by-同舟云学术

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

Published:2008-11-23 Issue:12 Volume:40 Page:1466-1471
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Brunetti-Pierri Nicola,Berg Jonathan S,Scaglia Fernando,Belmont John,Bacino Carlos A,Sahoo Trilochan,Lalani Seema R,Graham Brett,Lee Brendan,Shinawi Marwan,Shen Joseph,Kang Sung-Hae L,Pursley Amber,Lotze Timothy,Kennedy Gail,Lansky-Shafer Susan,Weaver Christine,Roeder Elizabeth R,Grebe Theresa A,Arnold Georgianne L,Hutchison Terry,Reimschisel Tyler,Amato Stephen,Geragthy Michael T,Innis Jeffrey W,Obersztyn Ewa,Nowakowska Beata,Rosengren Sally S,Bader Patricia I,Grange Dorothy K,Naqvi Sayed,Garnica Adolfo D,Bernes Saunder M,Fong Chin-To,Summers Anne,Walters W David,Lupski James R,Stankiewicz Pawel,Cheung Sau Wai,Patel Ankita

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.279.pdf

Reference25 articles.

1. Christiansen, J. et al. Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease. Circ. Res. 94, 1429–1435 (2004).

2. Sharp, A.J. et al. Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome. Nat. Genet. 38, 1038–1042 (2006).

3. Shaffer, L.G. et al. Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases. J. Pediatr. 149, 98–102 (2006).

4. Stefansson, H. et al. Large recurrent microdeletions associated with schizophrenia. Nature 455, 232–236 (2008).

5. Stone, J.L. et al. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455, 237–241 (2008).

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