Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.
about
Fragile X syndrome: the FMR1 CGG repeat distribution among world populationsGenetics. Toward a new vocabulary of human genetic variationPatterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms.Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.FMR1 gene and fragile X syndrome.Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population.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.Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes.Expansion of an FMR1 grey-zone allele to a full mutation in two generations.Genetic polymorphisms of nine X-STR loci in four population groups from Inner Mongolia, China.FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability.Prevalence of the fragile X syndrome in African-Americans.Single nucleotide polymorphism and FMR1 CGG repeat instability in two Basque valleys.Extended single nucleotide polymorphism and haplotype analysis of the elastin gene in Caucasians with intracranial aneurysms provides evidence for racially/ethnically based differences.Contraction of fully expanded FMR1 alleles to the normal range: predisposing haplotype or rare events?AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations.A new insight into fragile X syndrome among Basque population.Distribution of CGG repeats and FRAXAC1/DXS548 alleles in South American populations.An exact test for the association between the disease and alleles at highly polymorphic loci with particular interest in the haplotype analysis.
P2860
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P2860
Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
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2000年學術文章
@zh-hant
name
Survey of the fragile X syndro ...... n African American population.
@en
Survey of the fragile X syndro ...... n African American population.
@nl
type
label
Survey of the fragile X syndro ...... n African American population.
@en
Survey of the fragile X syndro ...... n African American population.
@nl
prefLabel
Survey of the fragile X syndro ...... n African American population.
@en
Survey of the fragile X syndro ...... n African American population.
@nl
P2093
P2860
P356
P1476
Survey of the fragile X syndro ...... n African American population.
@en
P2093
C E Schwartz
D C Crawford
E M Rohlfs
G L Feldman
J L Newman
K G Monaghan
K L Meadows
N J Carpenter
P2860
P304
P356
10.1086/302762
P407
P50
P577
2000-02-01T00:00:00Z