(Q34733385)

4 August 2017

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title

A developmental approach to understanding Fragile X syndrome in females (English)

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4 August 2017

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2

Michèle M M Mazzocco

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4 August 2017

Cynthia S Keysor

1

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4 August 2017

publication date

1 May 2002

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Microscopy Research and Technique

4 August 2017

published in

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4 August 2017

volume

57

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4 August 2017

issue

3

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4 August 2017

page(s)

179-186

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

4 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Prevalence of the fragile X anomaly amongst autistic twins and singletons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Early developmental trajectories of males with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Neuropsychological profiles of FMR-1 premutation and full-mutation carrier females

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Verbal learning and memory among heterozygous fragile X females

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Behavior problems of young girls with fragile X syndrome: factor scores on the Conners' Parent's Questionnaire.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Advances in research on the fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Math learning disability and math LD subtypes: evidence from studies of Turner syndrome, fragile X syndrome, and neurofibromatosis type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Specific frontal lobe deficits among women with the fragile X gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Autistic behaviors among girls with fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Social functioning among girls with fragile X or Turner syndrome and their sisters

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

The prevalence of the FMR1 and FMR2 mutations among preschool children with language delay

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Brief report: autistic behaviors among children with fragile X or Rett syndrome: implications for the classification of pervasive developmental disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

No widespread psychological effect of the fragile X premutation in childhood: evidence from a preliminary controlled study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Contribution of the FMR1 gene mutation to human intellectual dysfunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Obstetrical and gynecological complications in fragile X carriers: a multicenter study

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Symptoms of schizotypal personality disorder in fragile X women.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

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/10.1002%2FJEMT.10070

Population incidence and segregation ratios in the Martin-Bell syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Cognitive profiles of the carrier fragile X woman

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Abnormal behaviors of young girls with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

On the gates of hell and a most unusual gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Emotional and neurocognitive deficits in fragile X

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

Prevalence of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FJEMT.10070

21 January 2018

Identifiers

DOI

10.1002/JEMT.10070

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4 August 2017

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