(Q29039571)

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Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy

scientific article (publication date: 23 November 2003)

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Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy (English)

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27 March 2017

facioscapulohumeral muscular dystrophy

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Gert-Jan van Ommen

8

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Gert-Jan B van Ommen

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Silvère M van der Maarel

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Silvère M van der Maarel

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9

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Rune R Frants

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27 March 2017

George W. Padberg

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George W Padberg

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27 March 2017

author name string

Petra G M van Overveld

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27 March 2017

Richard J F L Lemmers

2

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27 March 2017

Lodewijk A Sandkuijl

3

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27 March 2017

Leo Enthoven

4

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27 March 2017

Sara T Winokur

5

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27 March 2017

Floor Bakels

6

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27 March 2017

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publication date

23 November 2003

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27 March 2017

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3

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Nature Genetics

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27 March 2017

35

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4

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315-317

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27 March 2017

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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7 January 2021

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Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease

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https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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Regulation of imprinting: A multi-tiered process

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https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

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https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

1 reference

https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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44th ENMC International Workshop: Facioscapulohumeral Muscular Dystrophy: Molecular Studies 19-21 July 1996, Naarden, The Netherlands

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7 January 2021

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Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1

1 reference

https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere

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https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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DNA methylation in health and disease

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https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene

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https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2.

1 reference

https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

based on heuristic

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Inappropriate Gene Activation in FSHD

1 reference

https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q

1 reference

https://api.crossref.org/works/10.1038%2FNG1262

7 January 2021

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27 March 2017

Consolidated OpenCitations Corpus – April 2017

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