(Q35197002)

English

Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded

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Europe PubMed Central

PubMed publication ID

7 August 2017

Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded (English)

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Europe PubMed Central

PubMed publication ID

7 August 2017

spinocerebellar ataxia

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based on heuristic

inferred from title

7

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H Y Zoghbi

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Europe PubMed Central

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7 August 2017

Bronya J. B. Keats

1

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B J Keats

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Europe PubMed Central

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7 August 2017

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M S Pollack

2

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Europe PubMed Central

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7 August 2017

A McCall

3

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Europe PubMed Central

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7 August 2017

M A Wilensky

4

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Europe PubMed Central

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7 August 2017

L J Ward

5

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Europe PubMed Central

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7 August 2017

M Lu

6

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7 August 2017

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publication date

1 November 1991

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7 August 2017

American Journal of Human Genetics

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7 August 2017

49

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7 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

972-977

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

1 reference

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13 July 2018

Inherited structural polymorphism of the fourth component of human complement

1 reference

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13 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Phenotyping of human complement component C4, a class-III HLA antigen

1 reference

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13 July 2018

Estimating the power of a proposed linkage study for a complex genetic trait.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Report of the committee on linkage and gene order

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

MAP, an expert system for multiple pairwise linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Dinucleotide repeat polymorphism at the D6S89 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

A mapping function for man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

13 July 2018

Letter: Hereditary ataxia and HL-A genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

26 September 2018

Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

26 September 2018

The simultaneous separation of the enzymes glyoxalase I, esterase D, and phosphoglucomutase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683235

26 September 2018

A family with hereditary ataxia: HLA typing

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia in a large kindred: age at onset, reproduction, and genetic linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coagulation factor XIII: a useful polymorphic genetic marker

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies in spinocerebellar ataxia (SCA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1928103

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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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