(Q24800026)

4 July 2017

title

Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients (English)

1 reference

4 July 2017

Tsuyoshi Matsumura

1

Tsuyoshi

Matsumura

1 reference

4 July 2017

Kanako Goto

2

Kanako

Goto

1 reference

4 July 2017

Gaku Yamanaka

3

Gaku

Yamanaka

1 reference

4 July 2017

Je Hyeon Lee

4

Je Hyeon

Lee

1 reference

4 July 2017

Cheng Zhang

5

Cheng

Zhang

1 reference

4 July 2017

Yukiko K Hayashi

6

Yukiko K

Hayashi

1 reference

4 July 2017

Kiichi Arahata

7

Kiichi

Arahata

1 reference

4 July 2017

language of work or name

English

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publication date

20 August 2002

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4 July 2017

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4 July 2017

volume

2

1 reference

4 July 2017

issue

1

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page(s)

7

1 reference

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

4 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1186/1471-2377-2-7

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

22 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122075

De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.

25 May 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122075

A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD).

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122075

Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122075

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=122075

DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-2-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-2-7

Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-2-7

Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-2-7

21 January 2018

Identifiers

DOI

10.1186/1471-2377-2-7

1 reference

Dimensions Publication ID

4 July 2017

0 references

1 reference

4 July 2017

1 reference