Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker. (Q40567709)

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9 October 2019

title

Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker (English)

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9 October 2019

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linkage disequilibrium

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H G Harley

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9 October 2019

J D Brook

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9 October 2019

J Floyd

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9 October 2019

S A Rundle

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9 October 2019

S Crow

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9 October 2019

K V Walsh

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9 October 2019

M C Thibault

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9 October 2019

P S Harper

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9 October 2019

D J Shaw

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9 October 2019

language of work or name

English

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publication date

1 July 1991

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2063878 AND SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

9 October 2019

published in

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9 October 2019

volume

49

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9 October 2019

issue

1

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9 October 2019

page(s)

68-75

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Strategies for multilocus linkage analysis in humans

9 October 2019

cites work

1 reference

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

22 September 2017

1 reference

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Human creatine kinase genes on chromosomes 15 and 19, and proximity of the gene for the muscle form to the genes for apolipoprotein C2 and excision repair

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Localization of a human Na ,K -ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Report of the committee on the genetic constitution of chromosomes 18 and 19.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

A polymorphic DNA clone which maps to 19q13.2-19qter (D19S62).

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

RFLP for a DNA clone which maps to 19q13.2-19qter (D19S63).

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Identification of new DNA markers close to the myotonic dystrophy locus

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Myotonic dystrophy in Quebec: geographical distribution and concept of genetic homogeneity

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Separation of large DNA molecules by contour-clamped homogeneous electric fields

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

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

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683213

Localisation of genetic markers and orientation of the linkage group on chromosome 19

15 June 2018

1 reference

12 December 2020

Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids

1 reference

12 December 2020

Further mapping of markers around the centromere of human chromosome 19

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12 December 2020

Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)

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12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2063878 AND SRC:MED&resulttype=core&format=json

9 October 2019

PubMed publication ID

2063878

1 reference