(Q24514983)

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Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families

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Europe PubMed Central

PubMed publication ID

1 July 2017

Evidence of genetic heterogeneity in the autosomal recessive adult forms of limb-girdle muscular dystrophy following linkage analysis with 15q probes in Brazilian families (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

1 reference

based on heuristic

inferred from title

limb-girdle muscular dystrophy

1 reference

based on heuristic

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Jean Weissenbach

5

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Jean Weissenbach

5

object named as

Weissenbach J

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1 July 2017

author name string

Passos-Bueno MR

1

1 reference

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1 July 2017

Richard I

2

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Europe PubMed Central

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1 July 2017

Vainzof M

3

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Europe PubMed Central

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1 July 2017

Fougerousse F

4

1 reference

Europe PubMed Central

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1 July 2017

Broux O

6

1 reference

Europe PubMed Central

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1 July 2017

Cohen D

7

1 reference

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1 July 2017

Akiyama J

8

1 reference

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1 July 2017

Marie SK

9

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1 July 2017

Carvalho AA

10

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1 July 2017

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publication date

1 May 1993

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1 July 2017

Journal of Medical Genetics

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1 July 2017

30

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Europe PubMed Central

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1 July 2017

5

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Europe PubMed Central

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1 July 2017

385-387

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

Strategies for multilocus linkage analysis in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016373

19 March 2017

An autosomal transcript in skeletal muscle with homology to dystrophin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016373

19 March 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=1016373

27 September 2017

A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016373

27 September 2017

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016373

27 September 2017

Estimate of the proportion of Duchenne muscular dystrophy with autosomal recessive inheritance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016373

30 May 2018

Linkage analysis in families with autosomal recessive limb-girdle muscular dystrophy (LGMD) and 6q probes flanking the dystrophin-related sequence.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016373

30 May 2018

Mapping of two chromosome 15 microsatellites

1 reference

https://pubmed.ncbi.nlm.nih.gov/8320700

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin immunostaining in muscles from patients with different types of muscular dystrophy: a Brazilian study

1 reference

https://pubmed.ncbi.nlm.nih.gov/8320700

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage

1 reference

https://pubmed.ncbi.nlm.nih.gov/8320700

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8320700

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human gene mapping 11. London Conference (1991). Eleventh International Workshop on Human Gene Mapping. London, UK, August 18-22, 1991

1 reference

https://pubmed.ncbi.nlm.nih.gov/8320700

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.30.5.385

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

OpenCitations bibliographic resource ID

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 July 2017

ResearchGate publication ID

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