Psychotic illness in people with Prader Willi syndrome due to chromosome 15 maternal uniparental disomy

Lancet

Volumn 359, Issue 9301, 2002, Pages 135-136

  Boer, Harm ^a   Holland, Anthony ^d   Whittington, Joyce ^d   Butler, Jill ^d   Webb, Tessa ^b   Clarke, David ^c  

^a North Warwickshire Trust   (United Kingdom)

^b BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^c North Warwickshire NHS Trust   (United Kingdom)

^d UNIVERSITY OF CAMBRIDGE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AFFECTIVE NEUROSIS; ARTICLE; CHROMOSOME 15; CHROMOSOME DELETION; CHROMOSOME MUTATION; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE EXPRESSION; HUMAN; MALE; MORBIDITY; ONSET AGE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

EID: 0037065539     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(02)07340-3     Document Type: Article

References (5)

1. Prader-Willi syndrome: Consensus diagnostic criteria
2. Prader-Willi syndrome and cycloid psychoses
3. Diagnostic tests for the Prader-Willi syndrome by SNURPN experession in blood
4. Population prevalence and estimated birth incidence and mortality rate for people with Prader-Willi syndrome in one UK Health Region
5. Depressive episodes in adults with learning disabilities