Sequence variation within the fragile X locus (Q35034541)

5 August 2017

title

Sequence variation within the fragile X locus (English)

1 reference

5 August 2017

D J Mathews

1

1 reference

5 August 2017

C Kashuk

2

1 reference

5 August 2017

G Brightwell

3

1 reference

5 August 2017

E E Eichler

4

1 reference

5 August 2017

A Chakravarti

5

1 reference

5 August 2017

language of work or name

1 reference

1 August 2001

1 reference

5 August 2017

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5 August 2017

volume

11

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5 August 2017

issue

8

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5 August 2017

page(s)

1382-1391

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The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models

5 August 2017

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8 July 2018

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8 July 2018

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DNA sequence variation in a non-coding region of low recombination on the human X chromosome

8 July 2018

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High polymorphism at the human melanocortin 1 receptor locus

8 July 2018

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8 July 2018

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X chromosome evidence for ancient human histories

8 July 2018

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

8 July 2018

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DNA variability and recombination rates at X-linked loci in humans

8 July 2018

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

8 July 2018

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The context of human genetic evolution

8 July 2018

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Consed: a graphical tool for sequence finishing

8 July 2018

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8 July 2018

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Base-calling of automated sequencer traces using phred. I. Accuracy assessment

8 July 2018

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Sequence variation in ZFX introns in human populations

8 July 2018

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Prediction of complete gene structures in human genomic DNA

8 July 2018

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Archaic African and Asian lineages in the genetic ancestry of modern humans

8 July 2018

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

8 July 2018

1 reference

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Coalescents and genealogical structure under neutrality.

8 July 2018

1 reference

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Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutation

8 July 2018

1 reference

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Absence of polymorphism at the ZFY locus on the human Y chromosome

8 July 2018

1 reference

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A recent common ancestry for human Y chromosomes

8 July 2018

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A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences

8 July 2018

1 reference

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Evolutionary relationship of DNA sequences in finite populations

8 July 2018

1 reference

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The neighbor-joining method: a new method for reconstructing phylogenetic trees

8 July 2018

1 reference

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On measures of gametic disequilibrium

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311115

A test of neutral molecular evolution based on nucleotide data

8 July 2018

1 reference

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DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis

8 July 2018

1 reference

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Statistical method for testing the neutral mutation hypothesis by DNA polymorphism

8 July 2018

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8 July 2018

1 reference

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Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers

8 July 2018

1 reference

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Adaptive protein evolution at the Adh locus in Drosophila

8 July 2018

1 reference

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On the number of segregating sites in genetical models without recombination

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311115

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

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=311115

Prospects for whole-genome linkage disequilibrium mapping of common disease genes

25 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11483579

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Population genetics--making sense out of sequence

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11483579

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11483579

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMC publication ID

311115

1 reference

5 August 2017

1 reference