(Q72213912)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7739624%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

title

The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7739624%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

2

C Wijmenga

1 reference

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24 October 2019

author name string

E Bakker

1

1 reference

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24 October 2019

R H Vossen

3

1 reference

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24 October 2019

G W Padberg

4

1 reference

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24 October 2019

J Hewitt

5

1 reference

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24 October 2019

M van der Wielen

6

1 reference

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24 October 2019

K Rasmussen

7

1 reference

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24 October 2019

R R Frants

8

1 reference

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24 October 2019

publication date

1 January 1995

1 reference

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24 October 2019

volume

2

1 reference

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24 October 2019

page(s)

S39-44

1 reference

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

24 October 2019

cites work

2 references

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

5 October 2024

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

1 reference

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy familes (FSHD) with 4q markers

1 reference

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

2 references

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

5 October 2024

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

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

2 references

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

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.

2 references

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

5 October 2024

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

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

1 reference

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

Centre d'etude du polymorphisme humain (CEPH): collaborative genetic mapping of the human genome

1 reference

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

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

2 references

5 October 2024

https://opencitations.net/index/api/v1/references/10.1002/MUS.880181309

5 October 2024

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

Identifiers

DOI

10.1002/MUS.880181309

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7739624%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

1 reference