Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY (Q57316260)

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scientific article published in The Lancet

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Language	Label	Description	Also known as
English	Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY	scientific article published in The Lancet

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

title

Xp21 DNA probe in diagnosis of muscular dystrophy and spinal muscular atrophy (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

main subject

spinal muscular atrophy

1 reference

based on heuristic

inferred from title

muscular atrophy

1 reference

based on heuristic

inferred from title

muscular dystrophy

1 reference

based on heuristic

inferred from title

author

John Burn

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

author name string

A Clarke

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

K E Davies

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

D Gardner-Medwin

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

P Hudgson

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

language of work or name

English

0 references

publication date

1 February 1989

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

published in

The Lancet

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

volume

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

issue

8635

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

page(s)

443

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

cites work

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990044-5

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990044-5

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Becker's X-linked muscular dystrophy histological, enzyme-histochemical, and ultrastructural studies of two cases, originally reported by Becker

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS0140-6736%2889%2990044-5

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S0140-6736(89)90044-5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

PubMed publication ID

2563824

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2563824

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2563824%20AND%20SRC:MED&resulttype=core&format=json

retrieved

1 October 2019

 

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