Minimal expression of myotonic dystrophy: a clinical and molecular analysis (Q33594628)

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scientific article published on November 1, 1992

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Language	Label	Description	Also known as
English	Minimal expression of myotonic dystrophy: a clinical and molecular analysis	scientific article published on November 1, 1992

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

title

Minimal expression of myotonic dystrophy: a clinical and molecular analysis (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

main subject

myotonic dystrophy

1 reference

based on heuristic

inferred from title

author name string

W. Reardon

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

H. G. Harley

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

J. D. Brook

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

S. A. Rundle

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

S. Crow

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

P. S. Harper

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

D. J. Shaw

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

language of work or name

English

0 references

publication date

1 November 1992

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

full work available at URL

https://europepmc.org/articles/PMC1016168

file format

HTML

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

https://europepmc.org/articles/PMC1016168?pdf=render

file format

Portable Document Format

online access status

open access

content deliverer

Europe PubMed Central

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1453424

retrieved

28 September 2022

published in

Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

volume

29

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

issue

11

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

page(s)

770-773

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1453424

retrieved

28 July 2017

cites work

Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers.

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=1016168

retrieved

21 June 2018

Myotonic dystrophy. Predictive value of normal results on clinical examination

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=1016168

retrieved

21 June 2018

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

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=1016168

retrieved

21 June 2018

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

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=1016168

retrieved

21 June 2018

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

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=1016168

retrieved

28 July 2018

Systemic treatment of early breast cancer by hormonal, cytotoxic, or immune therapy. 133 randomised trials involving 31,000 recurrences and 24,000 deaths among 75,000 women. Early Breast Cancer Trialists' Collaborative Group

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1453424

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1453424

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital dystrophia myotonica

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1453424

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Five years experience of predictive testing for myotonic dystrophy using linked DNA markers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1453424

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.29.11.770

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/znfdp4skpfcevhuk7roic3ietm

retrieved

30 July 2022

based on heuristic

mapped directly with Wikidata item

Fatcat ID

release_znfdp4skpfcevhuk7roic3ietm

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/znfdp4skpfcevhuk7roic3ietm

retrieved

30 July 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1016168

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/znfdp4skpfcevhuk7roic3ietm

retrieved

30 July 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1453424

1 reference

stated in

Fatcat

reference URL

https://api.fatcat.wiki/v0/release/znfdp4skpfcevhuk7roic3ietm

retrieved

30 July 2022

based on heuristic

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ResearchGate publication ID

21703143

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