Becker muscular dystrophy: correlation of deletion type with clinical severity (Q41670916)

6 October 2017

Becker muscular dystrophy: correlation of deletion type with clinical severity (English)

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Becker muscular dystrophy

6 October 2017

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Norman AM

1

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6 October 2017

Thomas NS

series ordinal

2

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6 October 2017

Kingston HM

series ordinal

3

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6 October 2017

Harper PS

series ordinal

4

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6 October 2017

language of work or name

English

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publication date

1 April 1990

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Journal of Medical Genetics

6 October 2017

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6 October 2017

27

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6 October 2017

4

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6 October 2017

236-239

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

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

Gene deletions in X-linked muscular dystrophy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

Dystrophin. The gene and its product

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017024

Localisation of gene for Becker muscular dystrophy

6 June 2018

1 reference

12 December 2020

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

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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

Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes

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12 December 2020

Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations

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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

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

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12 December 2020

Identifiers

DOI

10.1136/JMG.27.4.236

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release_jeukuqeq7beybgt7f5eac6zs4a

6 October 2017

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Fatcat

https://api.fatcat.wiki/v0/release/jeukuqeq7beybgt7f5eac6zs4a

24 November 2022

mapped directly with Wikidata item

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6 October 2017

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