Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115 (Q33597405)

28 July 2017

Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115 (English)

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28 July 2017

6

Zatz M

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28 July 2017

3

Love D

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28 July 2017

Passos-Bueno MR

1

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28 July 2017

Rapaport D

2

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28 July 2017

Flint T

4

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28 July 2017

Bortolini ER

5

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28 July 2017

Davies KE

7

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28 July 2017

language of work or name

English

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publication date

1 March 1990

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Journal of Medical Genetics

28 July 2017

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28 July 2017

27

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28 July 2017

3

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28 July 2017

145-150

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

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Clinical investigation in duchenne dystrophy: 2. Determination of the ?power? of therapeutic trials based on the natural history

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Duchenne and Becker muscular dystrophy mutations: analysis using 2.6 kb of muscle cDNA from the 5' end of the gene.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Partial gene duplication in Duchenne and Becker muscular dystrophies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Myopathy in complex glycerol kinase deficiency patients is due to 3' deletions of the dystrophin gene

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Detection of specific sequences among DNA fragments separated by gel electrophoresis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016994

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

14 July 2018

1 reference

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

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

Does unequal crossing over contribute to the mutation rate in Duchenne muscular dystrophy?

1 reference

12 December 2020

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

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12 December 2020

Identifiers

DOI

10.1136/JMG.27.3.145

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28 July 2017

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28 July 2017

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