A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus (Q35198392)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971149%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

title

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

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21 September 2019

1 reference

K Johnson

1

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21 September 2019

P Shelbourne

2

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21 September 2019

J Davies

3

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21 September 2019

J Buxton

4

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21 September 2019

E Nimmo

5

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21 September 2019

M J Siciliano

6

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21 September 2019

L L Bachinski

7

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21 September 2019

M Anvret

8

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21 September 2019

H Harley

9

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21 September 2019

S Rundle

10

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21 September 2019

language of work or name

English

0 references

publication date

1 June 1990

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971149%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

21 September 2019

published in

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21 September 2019

volume

46

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21 September 2019

page(s)

1073-1081

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21 September 2019

issue

6

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Assignment of the structural gene for the third component of human complement to chromosome 19.

21 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Strategies for multilocus linkage analysis in humans

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Removal of repeated sequences from hybridisation probes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Cloning of the chromosome translocation breakpoint junction of the t(14;19) in chronic lymphocytic leukemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Lorist6, a cosmid vector with BamHI, NotI, ScaI and HindIII cloning sites and altered neomycin phosphotransferase gene expression

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

A new probe for the diagnosis of myotonic muscular dystrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

NcoI RFLP at the human apolipoprotein CII gene locus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

A cosmid vector that facilitates restriction enzyme mapping

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Dimorphic markers for the human apolipoprotein CII gene locus

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

Involvement of cation transporting systems in myotonic diseases

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

A rapid alkaline extraction procedure for screening recombinant plasmid DNA

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683833

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

13 July 2018

1 reference

12 December 2020

Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19

1 reference

12 December 2020

Segregation analysis of myotonia atrophica

1 reference

12 December 2020

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

1 reference

12 December 2020

A DNA polymorphism adjacent to the human apolipoprotein CII gene

1 reference

12 December 2020

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

12 December 2020

A primary map of ten DNA markers and two serological markers for human chromosome 19

1 reference

12 December 2020

Criteria for establishing the validity of genetic recombination in myotonic dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

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

The locus for Japanese myotonic dystrophy is also linked to D19S19 on the long arm of chromosome 19

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1971149%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference