(Q51989177)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

title

The nature of the spatial deficit in young females with Fragile-X syndrome: a neuropsychological and molecular perspective (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

Fehmidah Munir

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

author name string

G Cross

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

publication date

1 November 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

volume

36

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

issue

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

page(s)

1239-1246

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

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

7 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

A classification of hand preference by association analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Short-term memory and cognitive variability in adult fragile X females.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Mental status and fragile X expression in relation to FMR-1 gene mutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Translational suppression by trinucleotide repeat expansion at FMR1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Neuropsychological dysfunction among affected heterozygous fragile X females

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

The right hemisphere: neuropsychological functions

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Specific frontal lobe deficits among women with the fragile X gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

A left hemisphere contribution to visuospatial processing.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

A profile of cognitive deficit in females from fragile X families.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Contribution of the FMR1 gene mutation to human intellectual dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Further segregation analysis of the fragile X syndrome with special reference to transmitting males

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Molecular/clinical correlations in females with fragile X.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

X-linked mental retardation, macro-orchidism, and the Xq27 fragile site

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Prevalence of fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

Fragile X genotype characterized by an unstable region of DNA.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0028-3932%2897%2900162-0

10.1016/S0028-3932(97)00162-0

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9842768%20AND%20SRC:MED&resulttype=core&format=json

7 December 2019

1 reference