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

30 November 2017

title

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

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30 November 2017

Mazzocco MM

1

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30 November 2017

Myers GF

2

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30 November 2017

Hamner JL

3

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30 November 2017

Panoscha R

4

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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

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The Journal of Pediatrics

30 November 2017

published in

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30 November 2017

volume

132

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30 November 2017

issue

5

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30 November 2017

page(s)

795-801

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The effectiveness of early intervention: a critical review

30 November 2017

cites work

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

7 January 2021

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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

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Identification of the gene FMR2, associated with FRAXE mental retardation

7 January 2021

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

7 January 2021

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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

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

7 January 2021

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

7 January 2021

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FRAXE and mental retardation

7 January 2021

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

7 January 2021

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Detection of full fragile X mutation

7 January 2021

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The FMR1 and FMR2 Mutations Are Not Common Etiologies of Academic Difficulty Among School-Age Children

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Prevalence of fragile X syndrome

7 January 2021

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Population studies of the fragile X: a molecular approach

7 January 2021

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Frequency and stability of the fragile X premutation

7 January 2021

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

7 January 2021

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10.1016/S0022-3476(98)70306-3

7 January 2021

Identifiers

DOI

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30 November 2017

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