(Q39813107)

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Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

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scholarly article

1 reference

Europe PubMed Central

14 September 2017

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population (English)

1 reference

Europe PubMed Central

14 September 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

short tandem repeat

1 reference

based on heuristic

inferred from title

fragile X syndrome

1 reference

based on heuristic

inferred from title

object named as

C Gunter

6

0 references

author name string

D C Crawford

1

1 reference

Europe PubMed Central

14 September 2017

C E Schwartz

2

1 reference

Europe PubMed Central

14 September 2017

K L Meadows

3

1 reference

Europe PubMed Central

14 September 2017

J L Newman

4

1 reference

Europe PubMed Central

14 September 2017

L F Taft

5

1 reference

Europe PubMed Central

14 September 2017

W T Brown

7

1 reference

Europe PubMed Central

14 September 2017

N J Carpenter

8

1 reference

Europe PubMed Central

14 September 2017

P N Howard-Peebles

9

1 reference

Europe PubMed Central

14 September 2017

K G Monaghan

10

1 reference

Europe PubMed Central

14 September 2017

S L Nolin

11

1 reference

Europe PubMed Central

14 September 2017

A L Reiss

12

1 reference

Europe PubMed Central

14 September 2017

G L Feldman

13

1 reference

Europe PubMed Central

14 September 2017

E M Rohlfs

14

1 reference

Europe PubMed Central

14 September 2017

S T Warren

15

1 reference

Europe PubMed Central

14 September 2017

S L Sherman

16

1 reference

Europe PubMed Central

14 September 2017

language of work or name

0 references

publication date

1 February 2000

1 reference

Europe PubMed Central

14 September 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

14 September 2017

66

1 reference

Europe PubMed Central

14 September 2017

2

1 reference

Europe PubMed Central

14 September 2017

480-493

1 reference

Europe PubMed Central

14 September 2017

Estimation of average heterozygosity and genetic distance from a small number of individuals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Estimating African American admixture proportions by use of population-specific alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Examination of factors associated with instability of the FMR1 CGG repeat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Familial transmission of the FMR1 CGG repeat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Fragile X gene instability: anchoring AGGs and linked microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Caucasian genes in American blacks: new data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Fragile-X syndrome: unique genetics of the heritable unstable element

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

Inheritance of the fragile X syndrome: size of the fragile X premutation is a major determinant of the transition to full mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

FMR1 in global populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

A complex mutable polymorphism located within the fragile X gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

Fragile X syndrome: linkage analysis in black and white populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

DNA methylation represses FMR-1 transcription in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

15 June 2018

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Estimating European admixture in African Americans by using microsatellites and a microsatellite haplotype (CD4/Alu).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Stability of the FMR1 CGG repeat in a Basque sample.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Survey of the fragile X syndrome and the fragile X E syndrome in a special education needs population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Examination of factors that influence the expansion of the fragile X mutation in a sample of conceptuses from known carrier females.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Population screening at the FRAXA and FRAXE loci: molecular analyses of boys with learning difficulties and their mothers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR test.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288101

20 August 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype analysis at the FRAXA locus in the Japanese population

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Robust amplification and ethidium-visible detection of the fragile X syndrome CGG repeat using Pfu polymerase

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of fragile X syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Precursor arrays for triplet repeat expansion at the fragile X locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10677308

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

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