(Q33597671)

28 July 2017

Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes (English)

1 reference

Becker muscular dystrophy

28 July 2017

1 reference

Cooke A

1

1 reference

28 July 2017

Lanyon WG

2

1 reference

28 July 2017

Wilcox DE

3

1 reference

28 July 2017

Dornan ES

4

1 reference

28 July 2017

Kataki A

5

1 reference

28 July 2017

Gillard EF

6

1 reference

28 July 2017

McWhinnie AJ

7

1 reference

28 July 2017

Morris A

8

1 reference

28 July 2017

Ferguson-Smith MA

9

1 reference

28 July 2017

Connor JM

10

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 May 1990

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

27

1 reference

28 July 2017

292-297

1 reference

28 July 2017

5

1 reference

Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mut

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017078

A deletion hot spot in the Duchenne muscular dystrophy gene

21 June 2018

1 reference

12 December 2020

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy

1 reference

12 December 2020

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1 reference

12 December 2020

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.27.5.292

1 reference

28 July 2017

1 reference

28 July 2017

1 reference