(Q48071488)

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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

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

author name string

Lyle R

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

Wright TJ

2

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

Clark LN

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

Hewitt JE

4

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

publication date

1 August 1995

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

28

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

3

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

389-397

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1093/HMG/3.8.1287

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1093/HMG/2.10.1667

Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1093/HMG/2.7.981

Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1038/NG0693-165

Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1093/HMG/2.10.1673

Molecular genetics of facioscapulohumeral muscular dystrophy

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1016/0960-8966(93)90102-P

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1038/NG0992-26

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

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1006/GENO.1994.1006

Identifiers

10.1006/GENO.1995.1166

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7490072

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