(Q45291147)

11 December 2017

title

Huntington disease in Finland: a molecular and genealogical study (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1351031

17 September 2022

0 references

0 references

1 reference

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restriction fragment length polymorphism

17 September 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1351031

17 September 2022

author name string

E. Ikonen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1351031

17 September 2022

J. Ignatius

2

1 reference

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17 September 2022

R. Norio

3

1 reference

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17 September 2022

J. Palo

4

1 reference

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17 September 2022

L. Peltonen

5

1 reference

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17 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1351031

17 September 2022

publication date

1 May 1992

1 reference

11 December 2017

1 reference

11 December 2017

volume

89

1 reference

11 December 2017

issue

3

1 reference

11 December 2017

page(s)

275-280

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00220539

11 December 2017

exact match

0 references

cites work

Recombination events suggest potential sites for the Huntington's disease gene

1 reference

12 December 2020

Cystic fibrosis in Finland: a molecular and genealogical study

1 reference

12 December 2020

The prevalence of Huntington's chorea in South Africa

1 reference

12 December 2020

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

12 December 2020

Studies on DNA markers (D4S10 and D4S43/S127) genetically linked to Huntington's disease in Japanese families

1 reference

12 December 2020

Low prevalence of Huntington's disease in Finland

1 reference

12 December 2020

Increased recombination adjacent to the Huntington disease-linked D4S10 marker

1 reference

12 December 2020

Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locus

1 reference

12 December 2020

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

12 December 2020

Linkage disequilibrium and modification of risk for Huntington disease

1 reference

12 December 2020

Huntington disease: no evidence for locus heterogeneity

1 reference

12 December 2020

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

12 December 2020

Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.

1 reference

12 December 2020

Huntington's chorea in Sweden

1 reference

12 December 2020

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene

1 reference

12 December 2020

Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy

1 reference

12 December 2020

Defined physical limits of the Huntington disease gene candidate region

1 reference

12 December 2020

A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients

1 reference

12 December 2020

Linkage disequilibrium in Huntington's disease: an improved localisation for the gene

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00220539

1 reference

Dimensions Publication ID

11 December 2017

1038166704

0 references

1 reference