(Q38554191)

4 September 2017

Discourse processing in women with fragile x syndrome: evidence for a deficit establishing coherence (English)

1 reference

4 September 2017

1 reference

J A Simon

1

1 reference

4 September 2017

J M Keenan

2

1 reference

4 September 2017

B F Pennington

3

1 reference

4 September 2017

A K Taylor

4

1 reference

4 September 2017

R J Hagerman

5

1 reference

4 September 2017

1 February 2001

1 reference

Cognitive Neuropsychology

4 September 2017

1 reference

4 September 2017

18

1 reference

4 September 2017

1

1 reference

4 September 2017

1-18

1 reference

Comprehension of humorous and nonhumorous materials by left and right brain-damaged patients

4 September 2017

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Surprise but not coherence: sensitivity to verbal humor in right-hemisphere patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Individual differences in working memory and reading

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Intelligence and the frontal lobe: the organization of goal-directed behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Chromosome fragility and psychopathology in obligate female carriers of the fragile X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

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/10.1080%2F02643290126042

Verbal learning and memory among heterozygous fragile X females

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Neuropsychological dysfunction among affected heterozygous fragile X females

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Speech disturbances (cluttering) in mildly impaired males with the Martin-Bell/fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Cognitive profiles of boys with the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

A unified account of cognitive impairments following frontal lobe damage: the role of working memory in complex, organized behavior.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Specific frontal lobe deficits among women with the fragile X gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Problem solving limitations among cytogenetically expressing fragile X women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

21 January 2018

Inference during reading

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

An exploration of right-hemisphere contributions to the pragmatic impairments of autism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Neurodevelopmental effects of the FMR-1 full mutation in humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Psychiatric disability in female carriers of the fragile X chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Normal phenotype in two brothers with a full FMR1 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Molecular/clinical correlations in females with fragile X.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Syntactic delay and pragmatic deviance in the language of fragile X males.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Neurobehavioral characteristics of CGG amplification status in fragile X females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

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/10.1080%2F02643290126042

Rapid antibody test for fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

A study of performance on tests from the CANTAB battery sensitive to frontal lobe dysfunction in a large sample of normal volunteers: Implications for theories of executive functioning and cognitive aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F02643290126042

21 January 2018

Identifiers

DOI

10.1080/02643290126042

1 reference

4 September 2017

1 reference