(Q45289537)

11 December 2017

title

Geographical distribution of haplotypes in Swedish families with Huntington's disease (English)

1 reference

11 December 2017

0 references

9

B Winblad

1 reference

11 December 2017

E Almqvist

1

1 reference

11 December 2017

S Andrew

2

1 reference

11 December 2017

J Theilmann

3

1 reference

11 December 2017

P Goldberg

4

1 reference

11 December 2017

J Zeisler

5

1 reference

11 December 2017

U Drugge

6

1 reference

11 December 2017

U Grandell

7

1 reference

11 December 2017

M Tapper-Persson

8

1 reference

11 December 2017

M Hayden

10

1 reference

11 December 2017

publication date

1 August 1994

1 reference

11 December 2017

1 reference

11 December 2017

volume

94

1 reference

11 December 2017

issue

2

1 reference

11 December 2017

page(s)

124-128

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00202856

11 December 2017

exact match

0 references

cites work

DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington disease

1 reference

12 December 2020

Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene

1 reference

12 December 2020

Huntington disease in Finland: a molecular and genealogical study

1 reference

12 December 2020

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expression

1 reference

12 December 2020

A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease

1 reference

12 December 2020

Low prevalence of Huntington's disease in Finland

1 reference

12 December 2020

A transcription map of the region containing the Huntington disease gene

1 reference

12 December 2020

Trinucleotide repeat elongation in the Huntingtin gene in Huntington disease patients from 71 Danish families

1 reference

12 December 2020

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

1 reference

12 December 2020

Expansion of the (CAG)n repeat causing Huntington's disease in 352 patients of German origin

1 reference

12 December 2020

Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.

1 reference

12 December 2020

Huntington disease without CAG expansion: phenocopies or errors in assignment?

1 reference

12 December 2020

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1 reference

12 December 2020

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

12 December 2020

Complex patterns of linkage disequilibrium in the Huntington disease region

1 reference

12 December 2020

A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing

1 reference

12 December 2020

Trinucleotide repeat length instability and age of onset in Huntington's disease

1 reference

12 December 2020

Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3.

1 reference

12 December 2020

Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number

1 reference

12 December 2020

The Huntington's disease candidate region exhibits many different haplotypes

1 reference

12 December 2020

Correlation between the onset age of Huntington's disease and length of the trinucleotide repeat in IT-15.

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00202856

1 reference

Dimensions Publication ID

11 December 2017

1044624342

0 references

1 reference