The prevalence of the FMR1 and FMR2 mutations among preschool children with language delay (Q44122161)

30 November 2017

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

1 reference

30 November 2017

Mazzocco MM

1

1 reference

30 November 2017

Myers GF

2

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30 November 2017

Hamner JL

3

1 reference

30 November 2017

Panoscha R

4

1 reference

30 November 2017

Shapiro BK

5

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30 November 2017

Reiss AL

6

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30 November 2017

language of work or name

English

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publication date

1 May 1998

1 reference

The Journal of Pediatrics

30 November 2017

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30 November 2017

132

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30 November 2017

5

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30 November 2017

795-801

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The effectiveness of early intervention: a critical review

30 November 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Effects of early intervention on cognitive function of low birth weight preterm infants

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

A simplified six-item checklist for screening for fragile X syndrome in the pediatric population.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

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%2FS0022-3476%2898%2970306-3

Identification of the gene FMR2, associated with FRAXE mental retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

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%2FS0022-3476%2898%2970306-3

Cognitive, behavioral, and neuroanatomical assessment of two unrelated male children expressing FRAXE.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

FRAXE and mental retardation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

On some technical aspects of direct DNA diagnosis of the fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Detection of full fragile X mutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

The FMR1 and FMR2 mutations are not common etiologies of academic difficulty among school-age children

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Brief screening questionnaire for determining affected state in fragile X syndrome: a consensus recommendation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Trinucleotide repeat expansion in the FRAXE locus is not common among institutionalized individuals with non-specific developmental disabilities.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Prevalence of fragile X syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Population studies of the fragile X: a molecular approach

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Frequency and stability of the fragile X premutation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

Hotspot for deletions in the CGG repeat region of FMR1 in fragile X patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970306-3

10.1016/S0022-3476(98)70306-3

7 January 2021

Identifiers

DOI

1 reference

30 November 2017

1 reference