(Q28250990)

1

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T Ikeuchi

2

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H Tanaka

4

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S Igarashi

5

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K Endo

6

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H Takahashi

7

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R Kondo

8

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A Ishikawa

9

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T Hayashi

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

10

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language of work or name

English

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publication date

January 1994

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published in

Nature Genetics

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volume

6

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issue

1

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page(s)

9-13

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0194-9

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0194-9

The gene for Machado-Joseph disease maps to human chromosome 14q

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0194-9

Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0194-9

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0194-9

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Unusual form of cerebellar ataxia; combined dentato-rubral and pallido-Luysian degeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

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

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Human genes containing polymorphic trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021

Supercoil sequencing: a fast and simple method for sequencing plasmid DNA

1 reference

https://api.crossref.org/works/10.1038%2FNG0194-9

7 January 2021