(Q40526312)

21 September 2017

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title

Genetics of learning disabilities (English)

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21 September 2017

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B F Pennington

1

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21 September 2017

publication date

1 January 1995

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Journal of Child Neurology

21 September 2017

published in

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21 September 2017

volume

10 Suppl 1

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21 September 2017

page(s)

S69-77

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Nature, nurture & psychology

21 September 2017

cites work

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https://api.crossref.org/works/10.1177%2F08830738950100S114

Learning disorders in children: sibling studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

The concept of specific reading retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

The genetics of specific reading disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Family history as an indicator of risk for reading disability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Evidence for a genetic aetiology in reading disability of twins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Evidence for major gene transmission of developmental dyslexia

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Commingling and segregation analysis of reading performance in families of normal reading probands.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Familial dyslexia: use of genetic linkage data to define subtypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

The Correlation between Relatives on the Supposition of Mendelian Inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Quantitative trait locus for reading disability on chromosome 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Specific frontal lobe deficits among women with the fragile X gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

Neuropsychology of early-treated phenylketonuria: specific executive function deficits

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738950100S114

10.1177/08830738950100S114

21 January 2018

Identifiers

DOI

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21 September 2017

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