(Q34606340)

3 August 2017

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title

Molecular diagnosis of facioscapulohumeral muscular dystrophy (English)

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facioscapulohumeral muscular dystrophy

3 August 2017

main subject

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author

David N. Cooper

series ordinal

2

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3 August 2017

Meena Upadhyaya

1

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3 August 2017

publication date

1 March 2002

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Expert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcare

3 August 2017

published in

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3 August 2017

volume

2

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3 August 2017

issue

2

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3 August 2017

page(s)

160-171

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Facioscapulohumeral muscular dystrophy

3 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

Profound misregulation of muscle-specific gene expression in facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1586%2F14737159.2.2.160

21 January 2018

Identifiers

DOI

10.1586/14737159.2.2.160

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3 August 2017

1 reference