Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population (Q43105676)

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scientific article published in January 1989

Language	Label	Description	Also known as
English	Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population	scientific article published in January 1989

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population (English)

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

myotonic dystrophy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

author name string

MacKenzie AE

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

MacLeod HL

2

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Hunter AG

3

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Korneluk RG

4

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

language of work or name

0 references

publication date

1 January 1989

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

44

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

1

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

140-147

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

Human apolipoproteins AI, AII, CII and CIII. cDNA sequences and mRNA abundance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

Allelic variation adjacent to the human insulin and apolipoprotein C-II genes in different ethnic groups.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

AvaII RFLP at the human apolipoprotein CII (APO CII) gene locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715447

25 May 2018

The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on the Genetic Constitution of Chromosomes 17, 18 and 19

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First-trimester prediction in fetus at risk for myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA banking: the effects of storage of blood and isolated DNA on the integrity of DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

INDIRECT CYSTIC FIBROSIS CARRIER DETECTION

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of apolipoprotein CII as a genetic marker for myotonic dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation analysis of myotonia atrophica

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA polymorphism adjacent to the human apolipoprotein CII gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/2562820

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 November 2017

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