Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population. (Q52472252)

From Wikidata

Jump to navigation Jump to search

scientific article published in October 1990

edit

Language	Label	Description	Also known as
English	Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.	scientific article published in October 1990

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

title

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

main subject

Finland

0 references

disequilibrium

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

author

Robert Winqvist

series ordinal

3

object named as

R Winqvist

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

author name string

P Nokelainen

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

L Alanen-Kurki

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

B Falck

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

H Somer

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

J Leisti

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

K Johnson

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

M L Savontaus

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

L Peltonen

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

publication date

1 October 1990

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

volume

85

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

issue

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

page(s)

541-545

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

cites work

A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Criteria for establishing the validity of genetic recombination in myotonic dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA polymorphism adjacent to the human apolipoprotein CII gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of polymorphism and linkage disequilibrium for cystic fibrosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary diseases in Finland; rare flora in rare soul

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NcoI RFLP at the creatine kinase-muscle type gene locus (CKMM, chromosome 19).

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NcoI and TaqI RFLPs for human M creatine kinase (CKM)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NcoI RFLP at the human apolipoprotein CII gene locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blot hybridisation analysis of genomic DNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1977684

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00194234

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

PubMed publication ID

1977684

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1977684

retrieved

2 May 2018

reference URL

http://europepmc.org/abstract/MED/1977684

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q52472252&oldid=2211642776"