Parental origin of Robertsonian translocation (15q22q) and Prader Willi syndrome associated with autism.

Arrieta, I; Lobato, M N; Martinez, B; Criado, B

Arrieta, I; Lobato, M N; Martinez, B; Criado, B.

Psychiatr Genet ; 4(1): 63-5, 1994.

Article in En | MEDLINE | ID: mdl-8049905

Subject(s)

Autistic Disorder/genetics; Chromosomes, Human, Pair 15; Prader-Willi Syndrome/genetics; Translocation, Genetic; Autistic Disorder/complications; Female; Humans; Male; Prader-Willi Syndrome/complications

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Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Autistic Disorder / Translocation, Genetic / Chromosomes, Human, Pair 15 Type of study: Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: Psychiatr Genet Journal subject: GENETICA / PSIQUIATRIA Year: 1994 Type: Article

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