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Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

http://www.wikidata.org/entity/Q47618055

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Rare structural variants in the DOCK8 gene identified in a cohort of 439 patients with neurodevelopmental disorders.Deletion at 12q12 increases the risk of developmental delay and intellectual disability

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Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

http://www.wikidata.org/entity/Q47618055

description

2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@en

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@nl

type

label

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@en

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@nl

prefLabel

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@en

Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@nl

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S11920-017-0831-5

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Current Psychiatry Reports

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Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?

@en

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Anne S Bassett

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Chelsea Lowther

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Danielle A Baribeau

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Gregory Costain

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P2860

Structural variation in the human genome

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Structural variation of chromosomes in autism spectrum disorder

Mechanisms underlying structural variant formation in genomic disorders

Advancing epilepsy genetics in the genomic era

Practical guidelines for managing adults with 22q11.2 deletion syndrome

Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes

Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.

Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

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s11920-017-0831-5

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82

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scholarly article

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10.1007/S11920-017-0831-5

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11

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2017-09-20T00:00:00Z

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28929285

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