Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome-Reference-Cited by-同舟云学术

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Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome

Published:2013-10-22 Issue:1 Volume:5 Page:
ISSN:1866-1947
Container-title:Journal of Neurodevelopmental Disorders
language:en
Short-container-title:J Neurodevelop Disord

Author:

Lukoshe Akvile,White Tonya,Schmidt Marcus N,van der Lugt Aad,Hokken-Koelega Anita C

Publisher

Springer Science and Business Media LLC

Subject

Cognitive Neuroscience,Neurology (clinical),Pathology and Forensic Medicine,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1186/1866-1955-5-31.pdf

Reference65 articles.

1. Soni S, Whittington J, Holland AJ, Webb T, Maina EN, Boer H, Clarke D: The phenomenology and diagnosis of psychiatric illness in people with Prader-Willi syndrome. Psychol Med. 2008, 38: 1505-1514.

2. Cassidy SB, Forsythe M, Heeger S, Nicholls RD, Schork N, Benn P, Schwartz S: Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15. Am J Med Genet. 1997, 68: 433-440. 10.1002/(SICI)1096-8628(19970211)68:4<433::AID-AJMG12>3.0.CO;2-T.

3. Ledbetter DH, Riccardi VM, Airhart SD, Strobel RJ, Keenan BS, Crawford JD: Deletions of chromosome 15 as a cause of the prader-willi syndrome. N Engl J Med. 1981, 304: 325-329. 10.1056/NEJM198102053040604.

4. Nicholls RD, Knoll JHM, Butler MG, Karam S, Lalande M: Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndrome. Nature. 1989, 342: 281-285. 10.1038/342281a0.

5. Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B: Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet. 1995, 9: 395-400. 10.1038/ng0495-395.

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