Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.
about
Fragile X syndrome: the FMR1 CGG repeat distribution among world populationsPhysical and genetic mapping of the serpin gene cluster at 14q32.1: allelic association and a unique haplotype associated with alpha 1-antitrypsin deficiencyDynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset.Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.The fragile x mental retardation syndrome 20 years after the FMR1 gene discovery: an expanding universe of knowledge.Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population.Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotypePhenotype correlation and intergenerational dynamics of the Friedreich ataxia GAA trinucleotide repeatHaplotypes and mutations in Wilson disease.Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosisGenetic linkage heterogeneity in myotubular myopathy.Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.Fragile X gene instability: anchoring AGGs and linked microsatellitesHaplotype studies in Wilson diseaseA multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.Linkage disequilibrium in the insulin gene region: size variation at the 5' flanking polymorphism and bimodality among "class I" alleles.Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations.FMR1 in global populationsLinkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutation.
P2860
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P2860
Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.
description
1993 nî lūn-bûn
@nan
1993 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1993 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
name
Linkage disequilibrium between ...... number of founder chromosomes.
@ast
Linkage disequilibrium between ...... number of founder chromosomes.
@en
type
label
Linkage disequilibrium between ...... number of founder chromosomes.
@ast
Linkage disequilibrium between ...... number of founder chromosomes.
@en
prefLabel
Linkage disequilibrium between ...... number of founder chromosomes.
@ast
Linkage disequilibrium between ...... number of founder chromosomes.
@en
P2093
P2860
P1476
Linkage disequilibrium between ...... number of founder chromosomes.
@en
P2093
Deluchat C
Lentes-Zengerling S
P2860
P304
P407
P577
1993-02-01T00:00:00Z