(Q38237407)

31 August 2017

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title

Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving field (English)

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Duchenne muscular dystrophy

31 August 2017

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Bakker E

1

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31 August 2017

Bonten EJ

2

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31 August 2017

Veenema H

3

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31 August 2017

den Dunnen JT

4

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31 August 2017

Grootscholten PM

5

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31 August 2017

van Ommen GJ

6

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31 August 2017

Pearson PL

7

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31 August 2017

1 January 1989

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31 August 2017

17

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Journal of Inherited Metabolic Disease

inferred from page(s)

published in

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31 August 2017

12 Suppl 1

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31 August 2017

174-190

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https://scigraph.springernature.com/pub.10.1007/bf01799293

31 August 2017

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cites work

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

Transcription of the dystrophin gene in human muscle and non-muscle tissue

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

Serum creatine kinase activity and carrier status for duchenne muscular dystrophy

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12 December 2020

Individual-specific ‘fingerprints’ of human DNA

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Gene studies in newborn males with Duchenne muscular dystrophy detected by neonatal screening

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12 December 2020

A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male

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12 December 2020

Conservation of the Duchenne muscular dystrophy gene in mice and humans

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12 December 2020

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

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12 December 2020

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure

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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 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

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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

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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

Effective strategy for prenatal prediction of Duchenne and Becker muscular dystrophy

1 reference

12 December 2020

Germline mosaicism and Duchenne muscular dystrophy mutations

1 reference

12 December 2020

Localisation of gene for Becker muscular dystrophy

1 reference

12 December 2020

Muscular dystrophy in girls with X;autosome translocations

1 reference

12 December 2020

Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

1 reference

12 December 2020

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

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

Identifiers

DOI

10.1007/BF01799293

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Dimensions Publication ID

31 August 2017

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1 reference