Relationship between the IQ of people with Prader-Willi syndrome and that of their siblings: evidence for imprinted gene effects
Author:
Publisher
Wiley
Subject
Psychiatry and Mental health,Clinical Neurology,Neurology,Arts and Humanities (miscellaneous),Rehabilitation
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2788.2009.01157.x/fullpdf
Reference21 articles.
1. Expression of four genes between chromosome 15 breakpoints 1 and 2 and behavioural outcomes in Prader-Willi syndrome;Bittel;Pediatrics,2006
2. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy;Butler;Pediatrics,2004
3. Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons;Chai;American Journal of Human Genetics,2003
4. Angelman syndrome: a review of the clinical and genetic aspects;Clayton-Smith;Journal of Medical Genetics,2003
5. Strengths and weaknesses in the cognitive profile of youngsters with Prader-Willi syndrome;Curfs;Clinical Genetics,1991
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