(Q40577449)

21 September 2017

Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene (English)

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Duchenne muscular dystrophy

21 September 2017

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Gillard EF

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21 September 2017

Chamberlain JS

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21 September 2017

Murphy EG

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21 September 2017

Duff CL

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21 September 2017

Smith B

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21 September 2017

Burghes AH

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21 September 2017

Thompson MW

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21 September 2017

Sutherland J

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21 September 2017

Oss I

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21 September 2017

Bodrug SE

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21 September 2017

language of work or name

English

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publication date

1 October 1989

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American Journal of Human Genetics

21 September 2017

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21 September 2017

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21 September 2017

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21 September 2017

507-520

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

21 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

A cosmid vector for systematic chromosome walking

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Normal human genomic restriction-fragment patterns and polymorphisms revealed by hybridization with the entire dystrophin cDNA.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Deletion of a DNA sequence in eight of nine families with X-linked ichthyosis (steroid sulphatase deficiency).

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Molecular deletion analysis in Duchenne muscular dystrophy.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

A cDNA clone from the Duchenne/Becker muscular dystrophy gene.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

Frame-shift deletions in patients with Duchenne and Becker muscular 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=1683502

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular 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=1683502

Unexpected relationships between four large deletions in the human beta-globin gene cluster

15 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683502

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

20 August 2018

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12 December 2020

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

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12 December 2020

DNA deletions in mild and severe Becker muscular dystrophy

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12 December 2020

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

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12 December 2020

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels

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12 December 2020

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

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12 December 2020

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene

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12 December 2020

Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion

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12 December 2020

Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

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12 December 2020

A deletion hot spot in the Duchenne muscular dystrophy gene

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12 December 2020

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

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12 December 2020

Patterns of exon deletions in Duchenne and Becker muscular dystrophy

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12 December 2020

Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy

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12 December 2020

Identifiers

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21 September 2017

PubMed publication ID

2491010

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