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Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes (Q35199415)

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scientific article published on March 1, 1992

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English	Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes	scientific article published on March 1, 1992

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scholarly article

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7 August 2017

Friedreich ataxia in Louisiana Acadians: demonstration of a founder effect by analysis of microsatellite-generated extended haplotypes (English)

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PubMed publication ID

7 August 2017

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Friedreich ataxia

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R. Fujita

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347194

16 September 2022

Bronya J. B. Keats

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B. Keats

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16 September 2022

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G. Sirugo

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16 September 2022

F. Duclos

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16 September 2022

K. Purohit

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16 September 2022

M. Koenig

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16 September 2022

J. L. Mandel

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16 September 2022

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1 March 1992

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https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1347194/pdf/?tool=EBI

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16 September 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1347194/?tool=EBI

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16 September 2022

https://europepmc.org/articles/PMC1684290

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16 September 2022

https://europepmc.org/articles/PMC1684290?pdf=render

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16 September 2022

American Journal of Human Genetics

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7 August 2017

50

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7 August 2017

3

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7 August 2017

559-566

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Genetic homogeneity at the Friedreich ataxia locus on chromosome 9

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

A human single-copy DNA probe (DR 47) detects a Taq I RFLP on chromosome 9 (D9S5).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Towards construction of a high resolution map of the mouse genome using PCR-analysed microsatellites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Identification of a hypervariable microsatellite polymorphism within D9S15 tightly linked to Friedrich's ataxia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 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=1684290

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Vector-Alu PCR: a rapid step in mapping cosmids and YACs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684290

13 July 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

"Acadian" and "classical" forms of Friedreich ataxia are most probably caused by mutations at the same locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/1347194

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/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of CpG islands in a physical map encompassing the Friedreich's ataxia locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping complex genetic traits in humans: new methods using a complete RFLP linkage map

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessive ataxia in Acadians and "Cajuns"

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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