Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population (Q38351697)

2 September 2017

title

Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population (English)

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2 September 2017

author name string

Dolores Garcia Arocena

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1

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2 September 2017

Katherine E Breece

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2

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2 September 2017

Paul J Hagerman

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3

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2 September 2017

publication date

7 August 2003

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2 September 2017

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2 September 2017

volume

113

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2 September 2017

issue

5

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2 September 2017

page(s)

371-376

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Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

2 September 2017

cites work

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12 December 2020

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

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Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles

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Dynamic mutation: possible mechanisms and significance in human disease

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Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.

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Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations

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Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function

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Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group

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

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The fragile X gene and its function

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The Fragile X mental retardation protein

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Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.

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Prevalence of fragile X syndrome

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Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients

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Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG-repeat

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Conservation of CGG region in FMR1 gene in mammals

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Prenatal diagnosis and carrier screening for fragile X by PCR.

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Evolution of the cryptic FMR1 CGG repeat

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A Proposed Test Battery and Constellations of Specific Behavioral Paradigms to Investigate the Behavioral Phenotypes of Transgenic and Knockout Mice

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A decade of molecular studies of fragile X syndrome

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

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Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability

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12 December 2020

Instability of a (CGG)98 repeat in the Fmr1 promoter.

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Mutational bias provides a model for the evolution of Huntington's disease and predicts a general increase in disease prevalence.

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Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium

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Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population

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12 December 2020

Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles

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12 December 2020

Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles

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12 December 2020

Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations

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Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome

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12 December 2020

Biological implications of the DNA structures associated with disease-causing triplet repeats

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12 December 2020

Fragile X gene instability: anchoring AGGs and linked microsatellites

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12 December 2020

Mosaicism in fragile X affected males.

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12 December 2020

Data on the CGG repeat at the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate

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12 December 2020

Genetic diversity at the FMR1 locus in the Indonesian population

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12 December 2020

Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR

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12 December 2020

Significance of linkage disequilibrium between the fragile X locus and its flanking markers

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12 December 2020

Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation

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12 December 2020

Screening for fragile X syndrome in women of reproductive age

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12 December 2020

Evolution of simple repeats in DNA and their relation to human disease

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12 December 2020

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

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12 December 2020

10.1007/S00439-003-0982-9

Identifiers

DOI

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Dimensions Publication ID

2 September 2017

1014412692

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