(Q70170466)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3030926%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

title

DNA deletions in mild and severe Becker muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3030926%20AND%20SRC:MED&resulttype=core&format=json

Becker muscular dystrophy

9 October 2019

main subject

1 reference

K A Hart

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3030926%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

S Hodgson

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3030926%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

A Walker

3

1 reference

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9 October 2019

C G Cole

4

1 reference

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9 October 2019

L Johnson

5

1 reference

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9 October 2019

V Dubowitz

6

1 reference

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9 October 2019

M Bobrow

7

1 reference

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9 October 2019

publication date

1 March 1987

1 reference

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9 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3030926%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

volume

75

1 reference

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9 October 2019

page(s)

281-285

1 reference

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9 October 2019

issue

3

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00281075

9 October 2019

exact match

0 references

cites work

DNA deletion in boy with Becker muscular dystrophy

1 reference

12 December 2020

Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Linkage studies in Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophy.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

The screening of Duchenne muscular dystrophy patients for submicroscopic deletions.

1 reference

12 December 2020

Clinical studies in benign (Becker type) X-linked muscular dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00281075

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3030926%20AND%20SRC:MED&resulttype=core&format=json

9 October 2019

1 reference