InterRett, a model for international data collection in a rare genetic disorder-Reference-Cited by-同舟云学术

InterRett, a model for international data collection in a rare genetic disorder

Published:2009-07 Issue:3 Volume:3 Page:639-659
ISSN:1750-9467
Container-title:Research in Autism Spectrum Disorders
language:en
Short-container-title:Research in Autism Spectrum Disorders

Author:

Louise Sandra,Fyfe Sue,Bebbington Ami,Bahi-Buisson Nadia,Anderson Alison,Pineda Mercé,Percy Alan,Zeev Bruria Ben,Wu Xi Ru,Bao Xinhua,Leod Patrick Mac,Armstrong Judith,Leonard Helen

Publisher

Elsevier BV

Subject

Psychiatry and Mental health,Clinical Psychology,Developmental and Educational Psychology

Reference55 articles.

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3. Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation;Archer;Journal of Medical Genetics,2007

4. FOXG1 is responsible for the congenital variant of Rett syndrome;Ariani;American Journal of Human Genetics,2008

5. Australian Bureau of Statistics. (2006). Australian and New Zealand standard classification of occupations. (From http://www.abs.gov.au/AUSSTATS/abs@.nsf/mf/1220.0).

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