An experimental study of executive function and social impairment in Cornelia de Lange syndrome.

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An experimental study of executive function and social impairment in Cornelia de Lange syndrome.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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An experimental study of execu ...... in Cornelia de Lange syndrome.

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An experimental study of execu ...... in Cornelia de Lange syndrome.

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An experimental study of execu ...... in Cornelia de Lange syndrome.

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P1476

An experimental study of execu ...... in Cornelia de Lange syndrome

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P2093

Chris Oliver

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Donna Reid

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Lisa Nelson

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P2860

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

HDAC8 mutations in Cornelia de Lange syndrome affect the cohesin acetylation cycle

Does the autistic child have a "theory of mind"?

Children with autism fail to orient to naturally occurring social stimuli.

NIPBL mutational analysis in 120 individuals with Cornelia de Lange syndrome and evaluation of genotype-phenotype correlations.

Mother-child play: children with Down syndrome and typical development.

Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.

Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization.

Behavioural phenotype of Cornelia de Lange syndrome.

Effects of sampling context on spontaneous expressive language in males with fragile X syndrome or Down syndrome

P2888

s11689-017-9213-x

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scholarly article

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10.1186/S11689-017-9213-X

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P433

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P478

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J Moss

Hayley Crawford

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2017-09-11T00:00:00Z

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1091251895

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28889797

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5592717

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