(Q35197608)

7 August 2017

title

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

1 reference

Becker muscular dystrophy

7 August 2017

main subject

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M Koenig

1

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7 August 2017

A H Beggs

2

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7 August 2017

M Moyer

3

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7 August 2017

S Scherpf

4

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7 August 2017

K Heindrich

5

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7 August 2017

T Bettecken

6

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7 August 2017

G Meng

7

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7 August 2017

C R Müller

8

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7 August 2017

M Lindlöf

9

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7 August 2017

H Kaariainen

10

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7 August 2017

A de la Chapellet

11

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7 August 2017

A Kiuru

12

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7 August 2017

M L Savontaus

13

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7 August 2017

H Gilgenkrantz

14

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7 August 2017

D Récan

15

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7 August 2017

J Chelly

16

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7 August 2017

J C Kaplan

17

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7 August 2017

A E Covone

18

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7 August 2017

N Archidiacono

19

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7 August 2017

G Romeo

20

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7 August 2017

S Liechti-Gailati

21

1 reference

7 August 2017

V Schneider

22

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7 August 2017

S Braga

23

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7 August 2017

H Moser

24

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7 August 2017

B T Darras

25

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7 August 2017

P Murphy

26

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7 August 2017

U Francke

27

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7 August 2017

J D Chen

28

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7 August 2017

G Morgan

29

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7 August 2017

M Denton

30

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7 August 2017

C R Greenberg

31

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7 August 2017

K Wrogemann

32

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7 August 2017

L A Blonden

33

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7 August 2017

M B van Paassen

34

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7 August 2017

G J van Ommen

35

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7 August 2017

L M Kunkel

36

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7 August 2017

language of work or name

English

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publication date

1 October 1989

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

45

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7 August 2017

issue

4

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7 August 2017

page(s)

498-506

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A cDNA clone from the Duchenne/Becker muscular dystrophy gene.

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

The chicken dystrophin cDNA: striking conservation of the C-terminal coding and 3' untranslated regions between man and chicken

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

Gene deletions in X-linked muscular dystrophy

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683519

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy

26 September 2018

1 reference

12 December 2020

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

1 reference

12 December 2020

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

12 December 2020

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene

1 reference

12 December 2020

A deletion hot spot in the Duchenne muscular dystrophy gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy

1 reference

12 December 2020

Identifiers

PMC publication ID

1683519

1 reference

7 August 2017

1 reference