(Q33674017)

English

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy (English)

1 reference

Europe PubMed Central

28 July 2017

muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

Thompson MW

1

1 reference

Europe PubMed Central

28 July 2017

Ray PN

2

1 reference

Europe PubMed Central

28 July 2017

Belfall B

3

1 reference

Europe PubMed Central

28 July 2017

Duff C

4

1 reference

Europe PubMed Central

28 July 2017

Logan C

5

1 reference

Europe PubMed Central

28 July 2017

Oss I

6

1 reference

Europe PubMed Central

28 July 2017

Worton RG

7

1 reference

Europe PubMed Central

28 July 2017

language of work or name

0 references

publication date

1 December 1986

1 reference

Europe PubMed Central

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

28 July 2017

23

1 reference

Europe PubMed Central

28 July 2017

548-555

1 reference

Europe PubMed Central

28 July 2017

6

1 reference

Europe PubMed Central

28 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

A strategy to reveal high-frequency RFLPs along the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Lambda Charon vectors (Ch32, 33, 34 and 35) adapted for DNA cloning in recombination-deficient hosts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Efficientin vitrosynthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

The genetic linkage map of the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Report of the Committee on the Genetic Constitution of the X and Y Chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Human X chromosome markers and Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Linkage analysis of a DNA polymorphism proximal to the Duchenne and Becker muscular dystrophy loci on the short arm of the X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mp18 and pUC19 vectors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Molecular deletion analysis in Duchenne muscular dystrophy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

The detection of carriers of benign (Becker-type) X-linked muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Carrier detection in Duchenne muscular dystrophy. Evidence from a study of obligatory carriers and mothers of isolated cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

21 June 2018

Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049836

30 October 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human gene map 1 December 1984

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9)

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy families

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical investigation in Duchenne dystrophy: V. Use of creatine kinase and pyruvate kinase in carrier detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the Committee on Human Gene Mapping by Recombinant DNA Techniques

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2879926

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.23.6.548

0 references

1 reference

Europe PubMed Central

28 July 2017

1 reference

Europe PubMed Central

28 July 2017

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