(Q85169940)

English

Confirmation that the specific SSLP microsatellite allele 4qA161 segregates with fascioscapulohumeral muscular dystrophy (FSHD) in a cohort of multiplex and simplex FSHD families

scientific article published on 01 November 2010

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Confirmation that the specific SSLP microsatellite allele 4qA161 segregates with fascioscapulohumeral muscular dystrophy (FSHD) in a cohort of multiplex and simplex FSHD families (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Fascioscapulohumeral Muscular Dystrophy

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based on heuristic

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author name string

Gillian Spurlock

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Hoi-Ping Jim

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

Meena Upadhyaya

3

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20928905

28 July 2024

publication date

1 November 2010

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmus.21766

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.21766

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

Muscle and Nerve

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

42

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

820-821

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease

1

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

2

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

3

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin

4

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

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

5

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere

6

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy

7

1 reference

10.1002/MUS.21766

https://api.crossref.org/works/10.1002/MUS.21766

28 July 2024

Identifiers

10.1002/MUS.21766

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20928905%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

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