Location of facioscapulohumeral muscular dystrophy gene on chromosome 4. (Q55052229)

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Language	Label	Description	Also known as
English	Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

title

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

main subject

facioscapulohumeral muscular dystrophy

0 references

author

Cisca Wijmenga

series ordinal

1

object named as

C Wijmenga

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

author name string

R R Frants

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

O F Brouwer

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

P Moerer

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

J L Weber

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

G W Padberg

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

language of work or name

English

0 references

publication date

1 September 1990

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

published in

The Lancet

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

volume

336

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

issue

8716

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

page(s)

651-653

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

cites work

Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5

2 references

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/citations/10.1016/0022-510X(90)90245-I

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Linkage studies in facioscapulohumeral muscular dystrophy

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Strategies for multilocus linkage analysis in humans

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Buffer gradient gels and 35S label as an aid to rapid DNA sequence determination

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophy

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Hearing loss in facioscapulohumeral dystrophy

1 reference

stated in

COCI

retrieved

5 October 2024

reference URL

https://opencitations.net/index/api/v1/references/10.1016/0140-6736(90)92148-B

Identifiers

DOI

10.1016/0140-6736(90)92148-B

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

PubMed publication ID

1975852

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1975852

retrieved

16 June 2018

reference URL

http://europepmc.org/abstract/MED/1975852

 

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