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English
Clinical evidence for heterogeneity in myotonic dystrophy
scientific article
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Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
title
Clinical evidence for heterogeneity in myotonic dystrophy
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
main subject
heterogeneity
1 reference
based on heuristic
inferred from title
myotonic dystrophy
1 reference
based on heuristic
inferred from title
author name string
Bundey S
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 October 1982
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
volume
19
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
page(s)
341-348
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
cites work
Early recognition of heterozygotes for the gene for dystrophia myotonica
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Genetic heterogeneity for dystrophia myotonica
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Early-onset dystrophia myotonica. Evidence supporting a maternal environmental factor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Congenital myotonic dystrophy in Britain. II. Genetic basis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Congenital myotonic dystrophy in Britain. I. Clinical aspects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Myotonia dystrophica: unusual features in a Labrador family
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Neonatal form of dystrophia myotonica. Five cases in preterm babies and a review of earlier reports
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1048918
retrieved
21 June 2018
Congenital dystrophia myotonica
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7143387
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1136/JMG.19.5.341
0 references
PMCID
1048918
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
PubMed ID
7143387
1 reference
stated in
Europe PubMed Central
PubMed ID
7143387
retrieved
28 July 2017
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