(Q47991794)

English

Genetic mapping of a second myotonic dystrophy locus

scientific article published in June 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Genetic mapping of a second myotonic dystrophy locus (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

myotonic dystrophy

1 reference

based on heuristic

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author name string

Ranum LP

1

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Rasmussen PF

2

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Benzow KA

3

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Koob MD

4

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Day JW

5

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

language of work or name

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publication date

1 June 1998

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Nature Genetics

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

19

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

2

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

196-198

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 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

https://api.crossref.org/works/10.1038%2F570

21 January 2018

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

Myotonic dystrophy reviewed: back to the future?

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

Myotonic dystrophy, knockouts, warts and all.

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

Mutation of human short tandem repeats

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2F570

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2F570

7 January 2021

based on heuristic

inferred from DOI database lookup

Myotonic dystrophy with no trinucleotide repeat expansion

1 reference

https://api.crossref.org/works/10.1038%2F570

7 January 2021

based on heuristic

inferred from DOI database lookup

Thornton-Griggs-Moxley disease: myotonic dystrophy type 2

1 reference

https://api.crossref.org/works/10.1038%2F570

7 January 2021

based on heuristic

inferred from DOI database lookup

Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts

1 reference

https://api.crossref.org/works/10.1038%2F570

7 January 2021

based on heuristic

inferred from DOI database lookup

Myotonic dystrophy phenotype without expansion of (CTG)n repeat: An entity distinct from proximal myotonic myopathy (PROMM)?

1 reference

https://api.crossref.org/works/10.1038%2F570

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 February 2018

http://europepmc.org/abstract/MED/9620781

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