Deletion screening in patients with Duchenne muscular dystrophy (Q69429412)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

title

Deletion screening in patients with Duchenne muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

Duchenne muscular dystrophy

1 October 2019

main subject

1 reference

K Wulff

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

F H Herrmann

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

M C Wapenaar

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

M Wehnert

series ordinal

4

1 reference

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1 October 2019

publication date

1 December 1989

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1 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

volume

236

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2614492%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

issue

8

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1 October 2019

page(s)

470-473

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Human X chromosome markers and Duchenne muscular dystrophy

1 October 2019

cites work

1 reference

12 December 2020

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy

1 reference

12 December 2020

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

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

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

1 reference

12 December 2020

Inherited deletion at Duchenne dystrophy locus in normal male

1 reference

12 December 2020

Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

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

1 reference

12 December 2020

Cloning of the breakpoint of an X;21 translocation associated with 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

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

1 reference

12 December 2020

Patterns of exon deletions in Duchenne and Becker muscular dystrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

Deletions of fetal and adult muscle cDNA in Duchenne and Becker muscular dystrophy patients

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