(Q57208554)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Analysis of deletions in three McLeod patients: exclusion of the XS locus from the Xp21.1-Xp21.2 region (English)

1 reference

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3 November 2019

2

1 reference

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3 November 2019

author name string

El Nemer W

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Collec E

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Gane P

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Cartron JP

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Kim CL

6

1 reference

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3 November 2019

publication date

1 February 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

International Journal of Immunogenetics

3 November 2019

published in

1 reference

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3 November 2019

volume

27

1 reference

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3 November 2019

issue

1

1 reference

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3 November 2019

page(s)

29-33

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3.

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2370.2000.00188.X

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2370.2000.00188.X

Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2370.2000.00188.X

Molecular basis and PCR-DNA typing of the Fya/fyb blood group polymorphism

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2370.2000.00188.X

McLeod syndrome: a distinct form of neuroacanthocytosis. Report of two cases and literature review with emphasis on neuromuscular manifestations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2370.2000.00188.X

10.1046/J.1365-2370.2000.00188.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10651848%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference