Chromosome 22q11 deletions and severe learning disability [10]

British Journal of Psychiatry

Volumn 179, Issue NOV., 2001, Pages 466-467

  Jones, R G ^a   Morley Canellas, J ^a   Owen, M J ^a   Murphy, K C ^a  

^a ABERTAWE BRO MORGANNWG UNIVERSITY HEALTH BOARD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

NEUROLEPTIC AGENT;

ADULT; BEHAVIOR THERAPY; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; CHROMOSOME DELETION 22; CLINICAL FEATURE; DISEASE COURSE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; HUMAN; LEARNING DISORDER; LETTER; PREVALENCE; PSYCHOSIS; VELOCARDIOFACIAL SYNDROME;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; LEARNING DISORDERS; MIDDLE AGED; SYNDROME;

EID: 0035185830     PISSN: 00071250     EISSN: None     Source Type: Journal    
DOI: 10.1192/bjp.179.5.466     Document Type: Letter

References (2)

1. Chromosome 22q11 deletions. An under-recognised cause of idiopathic learning disability