Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability-Reference-Cited by-同舟云学术

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Published:2006-08-13 Issue:9 Volume:38 Page:1032-1037
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Shaw-Smith Charles,Pittman Alan M,Willatt Lionel,Martin Howard,Rickman Lisa,Gribble Susan,Curley Rebecca,Cumming Sally,Dunn Carolyn,Kalaitzopoulos Dimitrios,Porter Keith,Prigmore Elena,Krepischi-Santos Ana C V,Varela Monica C,Koiffmann Celia P,Lees Andrew J,Rosenberg Carla,Firth Helen V,de Silva Rohan,Carter Nigel P

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1858.pdf

Reference29 articles.

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2. Shaw-Smith, C. et al. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features. J. Med. Genet. 41, 241–248 (2004).

3. Cheung, S.W. et al. Development and validation of a CGH microarray for clinical cytogenetic diagnosis. Genet. Med. 7, 422–432 (2005).

4. Rosenberg, C. et al. Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents. J. Med. Genet. 43, 180–186 (2006).

5. Stefansson, H. et al. A common inversion under selection in Europeans. Nat. Genet. 37, 129–137 (2005).

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