(Q69737086)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2784778%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

title

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2784778%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

1 reference

S Liechti-Gallati

1

1 reference

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5 October 2019

M Koenig

2

1 reference

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5 October 2019

L M Kunkel

3

1 reference

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5 October 2019

D Frey

4

1 reference

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5 October 2019

E Boltshauser

5

1 reference

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5 October 2019

V Schneider

6

1 reference

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5 October 2019

S Braga

7

1 reference

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5 October 2019

H Moser

8

1 reference

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5 October 2019

publication date

1 March 1989

1 reference

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5 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2784778%20AND%20SRC:MED&resulttype=core&format=json

5 October 2019

volume

81

1 reference

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5 October 2019

issue

4

1 reference

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5 October 2019

page(s)

343-348

1 reference

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Familial deletion in Becker type muscular dystrophy within the pXJ region

5 October 2019

cites work

1 reference

12 December 2020

Prenatal diagnosis and detection of carriers with DNA probes in Duchenne's muscular dystrophy

1 reference

12 December 2020

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

1 reference

12 December 2020

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

1 reference

12 December 2020

A deletion hot spot in the Duchenne muscular dystrophy gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular deletion analysis in Duchenne muscular dystrophy.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion

1 reference

12 December 2020

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

1 reference

12 December 2020

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

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

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

1 reference

12 December 2020

Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy

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

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

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

Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism

1 reference

12 December 2020

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

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

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

12 December 2020

A cDNA clone from the Duchenne/Becker muscular dystrophy gene

1 reference

12 December 2020

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

1 reference

12 December 2020

Duchenne muscular dystrophy: high frequency of deletions

1 reference

12 December 2020

Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia

1 reference

12 December 2020

An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.

1 reference

12 December 2020

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families

1 reference

12 December 2020

Localisation of gene for Becker muscular dystrophy

1 reference

12 December 2020

Molecular diagnosis of Duchenne and Becker muscular dystrophies. Current data

1 reference

12 December 2020

Muscular dystrophy in girls with X;autosome translocations

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

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

1 reference

12 December 2020

Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA

1 reference

12 December 2020