(Q35889037)

English

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes

scientific article published in March 1994

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomes (English)

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

author name string

Decorte R

1

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Wu R

2

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Marynen P

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

Cassiman JJ

4

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

language of work or name

0 references

publication date

1 March 1994

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

54

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

3

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

506-515

1 reference

Europe PubMed Central

PMC publication ID

10 August 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=1918131

11 July 2018

Heteroduplex analysis can increase the informativeness of PCR-amplified VNTR markers: application using a marker tightly linked to the COL2A1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Characterization of the COL2A1 VNTR polymorphism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

The sampling theory of selectively neutral alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Two highly polymorphic minisatellites from the pseudoautosomal region of the human sex chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Amplification of human minisatellites by the polymerase chain reaction: towards DNA fingerprinting of single cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Population amalgamation and genetic variation: observations on artificially agglomerated tribal populations of Central and South America

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Rapid typing of tandemly repeated hypervariable loci by the polymerase chain reaction: application to the apolipoprotein B 3' hypervariable region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Physical mapping of the human pseudo-autosomal region; comparison with genetic linkage map.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Mitochondrial DNA polymorphism reveals hidden heterogeneity within some Asian populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Strong linkage disequilibrium between the XY274 polymorphism and the pseudoautosomal boundary.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Direct electrophoretic detection of the allelic state of single DNA molecules in human sperm by using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Minisatellite repeat coding as a digital approach to DNA typing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Amplification and characterization of the retinoblastoma gene VNTR by PCR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Fixed-bin analysis for statistical evaluation of continuous distributions of allelic data from VNTR loci, for use in forensic comparisons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Characterization and rapid analysis of the highly polymorphic VNTR locus D4S125 (YNZ32), closely linked to the Huntington disease gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Analysis of the VNTR locus D1S80 by the PCR followed by high-resolution PAGE

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Performing the exact test of Hardy-Weinberg proportion for multiple alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

11 July 2018

Anomalous electrophoresis of deoxyribonucleic acid restriction fragments on polyacrylamide gels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

24 September 2018

Concept of VNTR alleles: Comparison of apolipoprotein B 3′ hypervariable region genotyping results obtained by three methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918131

24 September 2018

A gradient of sex linkage in the pseudoautosomal region of the human sex chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8116620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid detection of hypervariable regions by the polymerase chain reaction technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/8116620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8116620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8116620

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

10 August 2017

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