Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis (Q35246977)

7 August 2017

title

Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis (English)

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Duchenne muscular dystrophy

7 August 2017

main subject

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Ward PA

1

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7 August 2017

Hejtmancik JF

2

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7 August 2017

Witkowski JA

3

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7 August 2017

Baumbach LL

4

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7 August 2017

Gunnell S

5

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7 August 2017

Speer J

6

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7 August 2017

Hawley P

7

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7 August 2017

Tantravahi U

8

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7 August 2017

Caskey CT

9

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7 August 2017

language of work or name

English

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publication date

1 February 1989

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

volume

44

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7 August 2017

issue

2

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7 August 2017

page(s)

270-281

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

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=1715396

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Expression of the murine Duchenne muscular dystrophy gene in muscle and brain

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Prenatal testing for Duchenne and Becker muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Muscle histology and creatine kinase levels in the foetus in Duchenne muscular dystrophy

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

Germline mosaicism and Duchenne muscular dystrophy mutations

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715396

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

15 November 2018

1 reference

12 December 2020

Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy

1 reference

12 December 2020

Long-range restriction map around the Duchenne muscular dystrophy gene

1 reference

12 December 2020

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

1 reference

12 December 2020

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

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

DMD carrier detection and prenatal diagnosis via recombinant DNA methods

1 reference

12 December 2020

A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome

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

Variability of serum creatine phosphokinase activity in normal women and carriers of the gene for Duchenne muscular dystrophy

1 reference

12 December 2020

Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy

1 reference

12 December 2020

Failure of Fetal Creatine Phosphokinase as a Diagnostic Indicator of Duchenne Muscular Dystrophy

1 reference

12 December 2020

Sporadic occurrence of Duchenne muscular dystrophy: evidence for new mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome

1 reference

12 December 2020

Identifiers

PMC publication ID

1715396

1 reference

7 August 2017

1 reference