(Q34616225)

3 August 2017

title

Genetic linkage of Werner's syndrome to five markers on chromosome 8 (English)

1 reference

13 November 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1741060

13 November 2022

Goto M

1 reference

3 August 2017

Rubenstein M

1 reference

3 August 2017

Weber J

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3 August 2017

Woods K

1 reference

3 August 2017

Drayna D

1 reference

3 August 2017

language of work or name

English

0 references

publication date

1 February 1992

1 reference

3 August 2017

20 February 1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1741060

full work available at URL

13 November 2022

http://www.nature.com/articles/355735a0

1 reference

http://www.nature.com/articles/355735a0.pdf

13 November 2022

file format

Portable Document Format

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13 November 2022

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3 August 2017

volume

355

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3 August 2017

issue

6362

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3 August 2017

page(s)

735-738

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A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

3 August 2017

cites work

1 reference

7 January 2021

Werner's syndrome: a review of recent research with an analysis of connective tissue metabolism, growth control of cultured cells, and chromosomal aberrations

1 reference

7 January 2021

[Werner's syndrome and arteriosclerosis]

1 reference

7 January 2021

Low glucose-6-phosphate dehydrogenase activity in cultured skin fibroblasts from Werner's syndrome

1 reference

7 January 2021

Suppression of in vitro Epstein-Barr virus infection. A new role for adult human T lymphocytes

1 reference

7 January 2021

Urinary excretion of macromolecular acidic glycosaminoglycans in Werner's syndrome

1 reference

7 January 2021

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

7 January 2021

Localization of the spherocytosis gene to chromosome segment 8p11.22----8p21

1 reference

7 January 2021

Dinucleotide repeat polymorphisms at the D8S85, D8S87, and D8S88 loci

1 reference

7 January 2021

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

1 reference

7 January 2021

Dinucleotide repeat polymorphism at the human ankyrin gene (ANK1)

1 reference

7 January 2021

High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency

1 reference

7 January 2021

1 reference

7 January 2021

Human genes involved in lipolysis of plasma lipoproteins: mapping of loci for lipoprotein lipase to 8p22 and hepatic lipase to 15q21

1 reference

7 January 2021

Japanese Journal of Medicine

125

R Aoki

1988

1 reference

13 November 2022

Identifiers

DOI

10.1038/355735A0

1 reference

Dimensions Publication ID

3 August 2017

1037233144

0 references

Fatcat ID

release_ujv276dbb5e73c7sqvgf3ato2u

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ujv276dbb5e73c7sqvgf3ato2u

24 November 2022

mapped directly with Wikidata item

1 reference