Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.

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Neuropathology and animal models of autism: genetic and environmental factors Genetic insights into the functional elements of language.Towards a Better Molecular Diagnosis of FMR1-Related Disorders-A Multiyear Experience from a Reference Lab.

P2860

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P2860

Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.

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http://www.wikidata.org/entity/Q36132963

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2013 nî lūn-bûn

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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2013年论文

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2013年论文

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Identification of expanded all ...... nd Environment (CHARGE) study.

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Blythe Durbin-Johnson

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Federica Tassone

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Flora Tassone

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Isaac Pessah

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Nimrah S Choudhary

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Robin Hansen

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P2860

The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autism

Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of

Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X

Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Variation of the CGG repeat at the fragile X site results in genetic instability: resolution of the Sherman paradox

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

The role of AGG interruptions in the transcription of FMR1 premutation alleles

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism

The role of fragile X mental retardation protein in major mental disorders.

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s10803-012-1580-2

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530-539

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scholarly article

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10.1007/S10803-012-1580-2

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English

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Irva Hertz-Picciotto

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2013-03-01T00:00:00Z

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22767137

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autism

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4596818

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Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.

about

P2860

P2860

Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study.

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