(Q33494176)

27 July 2017

title

Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia (English)

1 reference

27 July 2017

1 reference

1 reference

linkage disequilibrium

1 reference

Fujita R

1 reference

27 July 2017

Hanauer A

1 reference

27 July 2017

Sirugo G

1 reference

27 July 2017

Heilig R

1 reference

27 July 2017

Mandel JL

1 reference

27 July 2017

language of work or name

English

0 references

publication date

1 March 1990

1 reference

Proceedings of the National Academy of Sciences of the United States of America

27 July 2017

published in

1 reference

27 July 2017

1 reference

27 July 2017

1 reference

27 July 2017

page(s)

1796-1800

1 reference

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

27 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

Chromosomal assignment of the genes for human aldehyde dehydrogenase-1 and aldehyde dehydrogenase-2

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

Genetic homogeneity at the Friedreich ataxia locus on chromosome 9

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

Isolation and mapping of a polymorphic DNA sequence pMCT112 on chromosome 9q (D9S15).

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone region

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

Identification of the cystic fibrosis gene: genetic analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53570

Clinical Description and Roentgenologic Evaluation of Patients with Friedreich's Ataxia

21 June 2018

1 reference

12 December 2020

Recessive ataxia in Acadians and "Cajuns"

1 reference

12 December 2020

The Quebec Cooperative Study of Friedreich's Ataxia: 1974-1984--10 years of research

1 reference

12 December 2020

Rapid RFLP screening procedure identifies new polymorphisms at albumin and alcohol dehydrogenase loci

1 reference

12 December 2020

Friedreich's ataxia in Kathikas-Arodhes, Cyprus

1 reference

12 December 2020

Mapping of mutation causing Friedreich's ataxia to human chromosome 9

1 reference

12 December 2020

Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker

1 reference

12 December 2020

Friedreich's ataxia: a clinical and genetic study of 90 families with an analysis of early diagnostic criteria and intrafamilial clustering of clinical features

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.87.5.1796

1 reference

27 July 2017

0 references

1 reference

27 July 2017

1 reference