A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q. (Q41671640)

6 October 2017

A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q. (English)

1 reference

6 October 2017

M Upadhyaya

1

1 reference

6 October 2017

P W Lunt

2

1 reference

6 October 2017

M Sarfarazi

3

1 reference

6 October 2017

W Broadhead

4

1 reference

6 October 2017

J Daniels

5

1 reference

6 October 2017

M Owen

6

1 reference

6 October 2017

P S Harper

7

1 reference

6 October 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

Journal of Medical Genetics

6 October 2017

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6 October 2017

28

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6 October 2017

10

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6 October 2017

665-671

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Easy calculations of lod scores and genetic risks on small computers

6 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Hearing loss in facioscapulohumeral dystrophy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Modern methods of diagnosis of muscle diseases.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Huntingtons disease: linkage with G8 on chromosome 4 and its consequences

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Linkage analysis of French families with facioscapulohumeral muscular dystrophy.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

A workshop on facioscapulohumeral (Landouzy-Déjérine) disease, Manchester, 16 to 17 November 1988

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

A genetic linkage study of facioscapulohumeral (Landouzy-Déjérine) disease with 24 polymorphic DNA probes

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Isolation and mapping of a polymorphic DNA sequence pH30 on chromosome 4[HGM provisional no. D4S139]

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

An autosomal transcript in skeletal muscle with homology to dystrophin

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Dinucleotide repeat polymorphism at the D4S171 locus

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Genetic counselling in facioscapulohumeral muscular dystrophy

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017052

A pedigree of hereditary progressive muscular dystrophy

16 June 2018

1 reference

12 December 2020

Evidence against location of the gene for facioscapulohumeral muscular dystrophy on the distal long arm of chromosome 14

1 reference

12 December 2020

Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophy

1 reference

12 December 2020

Linkage studies in facioscapulohumeral muscular dystrophy

1 reference

12 December 2020

DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.28.10.665

1 reference

6 October 2017

1 reference

6 October 2017

PubMed publication ID

1941963

1 reference