A survey of FRAXE allele sizes in three populations. - Wikidata - wikimedia - TriplyDB

A survey of FRAXE allele sizes in three populations.

A survey of FRAXE allele sizes in three populations.

http://www.wikidata.org/entity/Q52200257

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Microdeletions in FMR2 may be a significant cause of premature ovarian failure Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.FRAXA and FRAXE: the results of a five year survey.Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission.Fragile X founder effects and new mutations in Finland.A new PCR assay useful for screening of FRAXE/FMR2 mental impairment among males.Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians.Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997.Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.

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P2860

A survey of FRAXE allele sizes in three populations.

http://www.wikidata.org/entity/Q52200257

description

1996 nî lūn-bûn

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1996年の論文

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1996年学术文章

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1996年学术文章

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1996年學術文章

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1996年學術文章

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name

A survey of FRAXE allele sizes in three populations.

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A survey of FRAXE allele sizes in three populations.

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type

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A survey of FRAXE allele sizes in three populations.

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A survey of FRAXE allele sizes in three populations.

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prefLabel

A survey of FRAXE allele sizes in three populations.

@en

A survey of FRAXE allele sizes in three populations.

@nl

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American Journal of Medical Genetics Part A

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A survey of FRAXE allele sizes in three populations.

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P2093

Brown WT

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Curley D

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Dobkin C

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Ju W

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Kajanoja E

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Liu X

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Pang C

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P2860

FRAXE and mental retardation.

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

An n-allele model for progressive amplification in the FMR1 locus

Dynamic mutations: a new class of mutations causing human disease.

Population genetics of the fragile-X syndrome: multiallelic model for the FMR1 locus.

Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutation.

Length of uninterrupted CGG repeats determines instability in the FMR1 gene.

Triplet repeat expansion mutations: the example of fragile X syndrome.

Lymphangiosarcoma in late-onset hereditary lymphedema: case report and nosological implications.

Identification of the FRAXE fragile site in two families ascertained for X linked mental retardation.

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415-419

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2

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