Do anomalies of handedness exist in children with Fragile-X syndrome? (Q50302744)

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scientific article published in January 1997

Language	Label	Description	Also known as
English	Do anomalies of handedness exist in children with Fragile-X syndrome?	scientific article published in January 1997

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

Do anomalies of handedness exist in children with Fragile-X syndrome? (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

fragile X syndrome

1 reference

based on heuristic

inferred from title

author name string

Cornish KM

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

Pilgram J

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

Shaw K

3

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

publication date

1 January 1997

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

91-101

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

Molecular-neurobehavioral associations in females with the fragile X full mutation.

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

A classification of hand preference by association analysis

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Fragile X syndrome in females with autism

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Hand preference and hand skill in children with autism

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Neuropsychological dimensions of the fragile X syndrome: support for a non-dominant hemisphere dysfunction hypothesis

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Cognitive profiles associated with the fra(X) syndrome in males and females.

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Hemispheric asymmetries and early infantile autism.

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Handedness in childhood autism shows a dissociation of skill and preference

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Fragile X syndrome: a unique mutation in man.

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Behavioral phenotype of fragile X syndrome: DSM-III-R autistic behavior in male children

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Pathological left-handedness: an explanatory model

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Left-handedness and early brain insult: an explanation

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Handedness patterns in autism suggest subtypes

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

The relationship of handedness to the cognitive, language, and visuo-spatial skills of autistic patients

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2F713754261

21 January 2018

Identifiers

10.1080/713754261

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/15513057

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