Subcortical Signatures of Hemizygosity and Psychosis in 22q11.2 Deletion Syndrome: Finding Common Ground in Rare Genetic Variation.

Eisenberg, Daniel P; Gregory, Michael D; Berman, Karen F

Eisenberg, Daniel P; Gregory, Michael D; Berman, Karen F.

Afiliação

Eisenberg DP; Clinical and Translational Neuroscience Branch, NIMH, Intramural Research Program, Bethesda, Md.
Gregory MD; Clinical and Translational Neuroscience Branch, NIMH, Intramural Research Program, Bethesda, Md.
Berman KF; Clinical and Translational Neuroscience Branch, NIMH, Intramural Research Program, Bethesda, Md.

Am J Psychiatry ; 177(7): 564-566, 2020 07 01.

Article em En | MEDLINE | ID: mdl-32605438

Assuntos

Aracnodactilia; Síndrome de DiGeorge; Síndrome de Marfan; Transtornos Psicóticos; Variação Genética; Humanos

Palavras-chave

22q11.2 Deletion Syndrome; Copy Number Variant; Neuroanatomy; Neurodevelopment; Psychosis; Schizophrenia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Síndrome de DiGeorge / Aracnodactilia / Síndrome de Marfan Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Revista: Am J Psychiatry Ano de publicação: 2020 Tipo de documento: Article

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