AUTS2 Syndrome in a 68-year-old female: Natural history and further delineation of the phenotype.

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AUTS2 Syndrome in a 68-year-old female: Natural history and further delineation of the phenotype.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

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AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

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Item

label

AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

@en

AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

@nl

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AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

@en

AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

@nl

P1476

AUTS2 Syndrome in a 68-year-ol ...... delineation of the phenotype.

@en

P2093

Ece Sengun

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Kanay Yararbas

http://www.w3.org/2001/XMLSchema#string

Serdar Kasakyan

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Yasemin Alanay

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P2860

A Draft Sequence of the Neandertal Genome

An RNA gene expressed during cortical development evolved rapidly in humans

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders

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

Function and regulation of AUTS2, a gene implicated in autism and human evolution

A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept.

Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.

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3231-3236

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scholarly article

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10.1002/AJMG.A.37882

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English

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P478

170

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2016-08-17T00:00:00Z

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27531620

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