The role of clinical phenotypes in understanding the genetics of obsessive-compulsive disorder

Journal of Psychosomatic Research

Volumn 61, Issue 3, 2006, Pages 359-364

  Eapen, Valsamma ^a   Pauls, David L ^b   Robertson, Mary May ^c  

^a UNITED ARAB EMIRATES UNIVERSITY   (United Arab Emirates)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

^c ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

Clinical phenotypes; Genetics; Obsessive compulsive disorder; Segregation analysis

Indexed keywords

ARTICLE; ENVIRONMENTAL FACTOR; GENE LOCUS; GENETIC ANALYSIS; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION; HEREDITY; HUMAN; MORBIDITY; OBSESSIVE COMPULSIVE DISORDER; PARENT; RISK ASSESSMENT; SEGREGATION ANALYSIS; SIBLING; STATISTICAL SIGNIFICANCE; TWINS;

FEMALE; HUMANS; MALE; OBSESSIVE-COMPULSIVE DISORDER; PHENOTYPE; PREVALENCE; TOURETTE SYNDROME;

EID: 33747820234     PISSN: 00223999     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpsychores.2006.07.021     Document Type: Article

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