(Q35644505)

English

A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination

scientific article published on August 1995

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scholarly article

1 reference

Europe PubMed Central

9 August 2017

A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination (English)

1 reference

Europe PubMed Central

9 August 2017

author name string

Blouin JL

1

1 reference

Europe PubMed Central

9 August 2017

Christie DH

2

1 reference

Europe PubMed Central

9 August 2017

Gos A

3

1 reference

Europe PubMed Central

9 August 2017

Lynn A

4

1 reference

Europe PubMed Central

9 August 2017

Morris MA

5

1 reference

Europe PubMed Central

9 August 2017

Ledbetter DH

6

1 reference

Europe PubMed Central

9 August 2017

Chakravarti A

7

1 reference

Europe PubMed Central

9 August 2017

Antonarakis SE

8

1 reference

Europe PubMed Central

9 August 2017

language of work or name

0 references

publication date

1 August 1995

1 reference

Europe PubMed Central

9 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

9 August 2017

57

1 reference

Europe PubMed Central

9 August 2017

2

1 reference

Europe PubMed Central

9 August 2017

388-394

1 reference

Europe PubMed Central

9 August 2017

A linkage between DNA markers on the X chromosome and male sexual orientation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Correlations between isochores and chromosomal bands in the human genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Physical mapping of chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Mammalian meiotic recombination: a reexamination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

A YAC clone map spanning 7.5 megabases of human chromosome band Xq28.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Cosmid assembly and anchoring to human chromosome 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

VNTR and microsatellite polymorphisms within the subtelomeric region of 7q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Chiasma distribution at diakinesis in the normal human male

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

A highly conserved repetitive DNA sequence, (TTAGGG)n, present at the telomeres of human chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

An interspersed repeated sequence specific for human subtelomeric regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Trisomy 21: association between reduced recombination and nondisjunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Isolation of an active human transposable element

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

The highest gene concentrations in the human genome are in telomeric bands of metaphase chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

12 July 2018

Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

25 September 2018

Molecular cloning of human telomeres in yeast.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

25 September 2018

Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801529

15 November 2018

Structure of the terminal 300 kb of DNA from human chromosome 21q

1 reference

https://pubmed.ncbi.nlm.nih.gov/7668265

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/7668265

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A "hot spot" of recombination coincides with an interstitial telomeric sequence in the Armenian hamster

1 reference

https://pubmed.ncbi.nlm.nih.gov/7668265

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of a pericentric inversion in mouse chromosome 8 implicates telomeres as promoters of meiotic recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/7668265

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Linkage Map of Human Chromosome 21: 43 PCR Markers at Average Intervals of 2.5 cM

1 reference

https://pubmed.ncbi.nlm.nih.gov/7668265

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination

1 reference

https://pubmed.ncbi.nlm.nih.gov/7668265

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

9 August 2017

1 reference

Europe PubMed Central

9 August 2017

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