New founder haplotypes at the myotonic dystrophy locus in southern Africa. (Q35642948)

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scientific article published on June 1995

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Language	Label	Description	Also known as
English	New founder haplotypes at the myotonic dystrophy locus in southern Africa.	scientific article published on June 1995

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

title

New founder haplotypes at the myotonic dystrophy locus in southern Africa (English)

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

main subject

Southern Africa

0 references

myotonic dystrophy

1 reference

based on heuristic

inferred from title

author name string

Goldman A

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

Ramsay M

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

Jenkins T

series ordinal

3

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

language of work or name

English

0 references

publication date

1 June 1995

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

published in

American Journal of Human Genetics

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

volume

56

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

issue

6

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

page(s)

1373-1378

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

cites work

Structure and genomic sequence of the myotonic dystrophy (DM kinase) gene

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=1801092

retrieved

12 July 2018

Characterization and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with 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=1801092

retrieved

12 July 2018

Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats

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=1801092

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12 July 2018

High resolution of human evolutionary trees with polymorphic microsatellites

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801092

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12 July 2018

Sampling variances of heterozygosity and genetic distance

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801092

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12 July 2018

Myotonic dystrophy. Part I. A genealogical study in the northern Transvaal.

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801092

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12 July 2018

Mitochondrial DNA and human evolution

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801092

retrieved

12 July 2018

ESR dating evidence for early modern humans at Border Cave in South Africa

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=1801092

retrieved

12 July 2018

African Populations and the Evolution of Human Mitochondrial DNA

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=1801092

retrieved

12 July 2018

An unstable triplet repeat in a gene related to myotonic muscular 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=1801092

retrieved

12 July 2018

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

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=1801092

retrieved

12 July 2018

Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations

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=1801092

retrieved

12 July 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=1801092

retrieved

12 July 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=1801092

retrieved

12 July 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=1801092

retrieved

27 July 2018

Myotonic dystrophy CTG repeats and the associated insertion/deletion polymorphism in human and primate populations

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=1801092

retrieved

15 November 2018

Ethnic distribution of myotonic dystrophy gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7762560

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/7762560

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of unstable DNA region in Japanese myotonic dystrophy patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7762560

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Origin of the expansion mutation in myotonic dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7762560

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7762560

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7762560

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1801092

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

PubMed publication ID

7762560

1 reference

stated in

Europe PubMed Central

PMC publication ID

1801092

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7762560%20AND%20SRC:MED&resulttype=core&format=json

retrieved

25 October 2019

 

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