(Q35246988)

English

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

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

spinocerebellar ataxia

1 reference

based on heuristic

inferred from title

1

object named as

H Y Zoghbi

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Stephen P. Daiger

4

object named as

S P Daiger

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

author name string

L A Sandkuyl

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

J Ott

3

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

M Pollack

5

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

W E O'Brien

6

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

A L Beaudet

7

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

language of work or name

0 references

publication date

1 February 1989

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

44

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

255-263

1 reference

Europe PubMed Central

PubMed publication ID

7 August 2017

Olivopontocerebellar atrophy. A review of 117 cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 July 2018

Deletion and amplification of the HGPRT locus in Chinese hamster cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 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=1715397

12 July 2018

The neuropathology of olivopontocerebellar atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 July 2018

An algorithm to improve the computational efficiency of genetic linkage analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 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=1715397

12 July 2018

Construction of a map of the short arm of human chromosome 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 July 2018

Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 July 2018

Haplotypes of the coagulation factor XIII A subunit locus in normal and deficient subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 July 2018

Restriction fragment length polymorphism of the HLA-DP subregion and correlations to HLA-DP phenotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

12 July 2018

Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715397

26 September 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=1715397

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=1715397

26 September 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on the Genetic Constitution of Chromosomes 5 and 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia: study of a large kindred. I. General information and genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

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/2563195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple scheme for the analysis of HLA linkages in pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A family with hereditary ataxia: HLA typing

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2563195

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

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q35246988&oldid=1621172915"