242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread (Q45120865)

9 December 2017

title

242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread (English)

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27 October 2022

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27 October 2022

3

J. T. den Dunnen

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Christine Van Broeckhoven

27 October 2022

8

object named as

C. van Broeckhoven

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27 October 2022

Jeffrey S Chamberlain

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object named as

J. Chamberlain

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27 October 2022

author name string

den Dunnen JT

3

1 reference

9 December 2017

van Broeckhoven C

8

1 reference

9 December 2017

L. A. Blonden

1

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27 October 2022

P. M. Grootscholten

2

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27 October 2022

E. Bakker

4

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27 October 2022

S. Abbs

5

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27 October 2022

M. Bobrow

6

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27 October 2022

C. Boehm

7

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27 October 2022

L. Baumbach

9

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27 October 2022

language of work or name

English

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1679746

27 October 2022

publication date

1 July 1991

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full work available at URL

9 December 2017

https://api.elsevier.com/content/article/PII:088875439190445K?httpAccept=text/xml

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https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

https://api.elsevier.com/content/article/PII:088875439190445K?httpAccept=text/plain

27 October 2022

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

27 October 2022

1 reference

9 December 2017

volume

10

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9 December 2017

issue

3

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9 December 2017

page(s)

631-639

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Molecular and clinical correlations of deletions leading to Duchenne and Becker muscular dystrophies

9 December 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.

27 October 2022

2

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

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

27 October 2022

4

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Matrix attachment regions are positioned near replication initiation sites, genes, and an interamplicon junction in the amplified dihydrofolate reductase domain of Chinese hamster ovary cells

27 October 2022

6

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

27 October 2022

8

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

27 October 2022

9

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies

27 October 2022

10

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

27 October 2022

12

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Molecular analysis of deletions in the human beta-globin gene cluster: deletion junctions and locations of breakpoints

27 October 2022

13

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Evidence for mutation by unequal sister chromatid exchange in the Duchenne muscular dystrophy gene

27 October 2022

14

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

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

27 October 2022

16

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

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

27 October 2022

17

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion

27 October 2022

18

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Mike, a chimeric filamentous phage designed for the separate production of either DNA strand of pKUN vector plasmids by F+ cells.

27 October 2022

19

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

A transcribed gene in an intron of the human factor VIII gene

27 October 2022

20

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

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

27 October 2022

21

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

27 October 2022

22

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Recombination at the human alpha-globin gene cluster: sequence features and topological constraints

27 October 2022

23

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocations

27 October 2022

24

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker

27 October 2022

27

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus.

27 October 2022

28

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

A deletion hot spot in the Duchenne muscular dystrophy gene

27 October 2022

29

1 reference

https://api.crossref.org/works/10.1016/0888-7543(91)90445-K

27 October 2022

Identifiers

1 reference

9 December 2017

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