(Q28247146)

English

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa

scientific article (publication date: April 1994)

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa (English)

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

0 references

0 references

muscular dystrophy

1 reference

based on heuristic

inferred from title

Jacques S Beckmann

10

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

author name string

F el Kerch

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

A Sefiani

2

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

K Azibi

3

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

N Boutaleb

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

M Yahyaoui

5

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

A Bentahila

6

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

M C Vinet

7

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

F Leturcq

8

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

L Bachner

9

1 reference

Europe PubMed Central

PMC publication ID

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24 October 2019

language of work or name

0 references

publication date

1 April 1994

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Journal of Medical Genetics

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

31

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

4

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

342-343

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

20 March 2017

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

7 April 2017

Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

29 September 2017

A second-generation linkage map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

29 September 2017

Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

29 September 2017

Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

2 June 2018

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

2 June 2018

Severe autosomal recessive muscular dystrophy in an extended Sudanese kindred.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049813

27 November 2018

Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries

1 reference

https://pubmed.ncbi.nlm.nih.gov/8071965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy: deficiency of dystrophin-associated proteins in the sarcolemma

1 reference

https://pubmed.ncbi.nlm.nih.gov/8071965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12

1 reference

https://pubmed.ncbi.nlm.nih.gov/8071965

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.31.4.342

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8071965%20AND%20SRC:MED&resulttype=core&format=json

24 October 2019

ResearchGate publication ID

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