Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses (Q28305523)

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English	Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses	scientific article

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scholarly article

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Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses (English)

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Huntington's disease

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author name string

S S Chong

1

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E Almqvist

2

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H Telenius

3

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L LaTray

4

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K Nichol

5

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B Bourdelat-Parks

6

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Y P Goldberg

7

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B R Haddad

8

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F Richards

9

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D Sillence

10

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C R Greenberg

11

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E Ives

12

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G Van den Engh

13

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M R Hughes

14

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M R Hayden

15

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language of work or name

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publication date

February 1997

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Human Molecular Genetics

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6

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2

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301-9

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

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https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

De novo expansion of a (CAG)n repeat in sporadic Huntington's disease

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https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Structure and expression of the Huntington's disease gene: evidence against simple inactivation due to an expanded CAG repeat

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Mutation analysis in patients with possible but apparently sporadic Huntington's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Parallel processing data acquisition system for multilaser flow cytometry and cell sorting

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Photo‐bleaching and photon saturation in flow cytometry

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.2.301

21 January 2018

Identifiers

10.1093/HMG/6.2.301

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