Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype
about
Genomic microsatellites identify shared Jewish ancestry intermediate between Middle Eastern and European populationsThe role of AGG interruptions in fragile X repeat expansions: a twenty-year perspectiveDevelopment of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion MutationsFMR1 CGG Repeats: Reference Levels and Race-Ethnic Variation in Women With Normal Fertility (Study of Women's Health Across the Nation).The economic burden of fragile x syndrome: healthcare resource utilization in the United States.Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel.Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.FMR1 and the fragile X syndrome: human genome epidemiology reviewFragile sites-cytogenetic similarity with molecular diversity.Distribution of AGG interruption patterns within nine world populations.Cascade Screening for Fragile X Syndrome/CGG Repeat Expansions in Children Attending Special Education in Sri Lanka.Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East.Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations.Unique AGG Interruption in the CGG Repeats of the FMR1 Gene Exclusively Found in Asians Linked to a Specific SNP HaplotypeAnalysis of the Fragile X Trinucleotide Repeat in Basques: Association of Premutation and Intermediate Sizes, Anchoring AGGs and Linked Microsatellites with Unstable Alleles.Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range.AGG interruptions within the maternal FMR1 gene reduce the risk of offspring with fragile X syndrome.Improved Assays for AGG Interruptions in Fragile X Premutation Carriers.Genetics and genomic medicine in Tunisia.
P2860
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P2860
Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype
description
1997 nî lūn-bûn
@nan
1997 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
name
Predisposition to the fragile ...... a rare Mediterranean haplotype
@ast
Predisposition to the fragile ...... a rare Mediterranean haplotype
@en
type
label
Predisposition to the fragile ...... a rare Mediterranean haplotype
@ast
Predisposition to the fragile ...... a rare Mediterranean haplotype
@en
prefLabel
Predisposition to the fragile ...... a rare Mediterranean haplotype
@ast
Predisposition to the fragile ...... a rare Mediterranean haplotype
@en
P2093
P2860
P1476
Predisposition to the fragile ...... a rare Mediterranean haplotype
@en
P2093
D L Nelson
E E Eichler
J N Macpherson
T C Falik-Zaccai
Z Borochowitz
P2860
P304
P407
P577
1997-01-01T00:00:00Z