An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

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An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

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An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

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An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

@en

An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

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An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

@en

An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

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P1476

An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.

@en

P2093

Chantal Missirian

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Clarisse Chatel

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François Poinso

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Jeremie Mortreux

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Jokthan Guivarch

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Nicole Philip

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Recurrence risk for autism spectrum disorders: a Baby Siblings Research Consortium study

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms.

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Segmental duplications mediate novel, clinically relevant chromosome rearrangements.

Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.

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s13256-018-1620-4

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scholarly article

case report

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10.1186/S13256-018-1620-4

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English

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P577

2018-03-18T00:00:00Z

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P6179

1101556513

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29549886

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P921

autism

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5857311

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