(Q34290105)

English

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy

scientific article

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy (English)

1 reference

Europe PubMed Central

1 August 2017

author name string

Meredith AL

1

1 reference

Europe PubMed Central

1 August 2017

Huson SM

2

1 reference

Europe PubMed Central

1 August 2017

Lunt PW

3

1 reference

Europe PubMed Central

1 August 2017

Sarfarazi M

4

1 reference

Europe PubMed Central

1 August 2017

Harley HG

5

1 reference

Europe PubMed Central

1 August 2017

Brook JD

6

1 reference

Europe PubMed Central

1 August 2017

Shaw DJ

7

1 reference

Europe PubMed Central

1 August 2017

Harper PS

8

1 reference

Europe PubMed Central

1 August 2017

language of work or name

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publication date

1 November 1986

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

293

1 reference

Europe PubMed Central

1 August 2017

1353-1356

1 reference

Europe PubMed Central

1 August 2017

6558

1 reference

Europe PubMed Central

1 August 2017

Early recognition of heterozygotes for the gene for dystrophia myotonica

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1342063

6 July 2018

Genetic linkage confirmed between the locus for myotonic dystrophy and the ABH-secretion and Lutheran blood group loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1342063

6 July 2018

The early detection of dystrophia myotonica

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1342063

6 July 2018

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1342063

6 July 2018

RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1342063

6 July 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2878705

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/2878705

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

https://pubmed.ncbi.nlm.nih.gov/2878705

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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