Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome (Q33670706)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6620324%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

title

Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6620324%20AND%20SRC:MED&resulttype=core&format=json

Becker muscular dystrophy

15 October 2019

main subject

1 reference

H M Kingston

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6620324%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

N S Thomas

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6620324%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

P L Pearson

3

1 reference

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15 October 2019

M Sarfarazi

4

1 reference

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15 October 2019

P S Harper

5

1 reference

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15 October 2019

language of work or name

English

0 references

publication date

1 August 1983

1 reference

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Journal of Medical Genetics

15 October 2019

published in

1 reference

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15 October 2019

volume

20

1 reference

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15 October 2019

issue

4

1 reference

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15 October 2019

page(s)

255-258

1 reference

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GLUCOSE-6-PHOSPHATE DEHYDROGENASE, COLOUR VISION AND XG BLOOD GROUPS IN GREECE: LINKAGE AND POPULATION DATA.

15 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

The application of DNA recombinant technology to the analysis of the human genome and genetic disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

A new era in mammalian gene mapping: somatic cell genetics and recombinant DNA methodologies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

Detection of specific sequences among DNA fragments separated by gel electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049115

The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups

30 October 2018

1 reference

12 December 2020

Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms

1 reference

12 December 2020

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

1 reference

12 December 2020

The human genome through the eyes of a clinical geneticist

1 reference

12 December 2020

[A new x-chromosomal muscular dystrophy]

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.20.4.255

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6620324%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6620324%20AND%20SRC:MED&resulttype=core&format=json

15 October 2019

PubMed publication ID

6620324

1 reference