(Q28261862)

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G Orozco

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J Weber

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L Heredero

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K Scheufler

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B Riley

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R Allotey

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C Nothers

Dominant spinopontine atrophy. Report of two additional members of family W

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language of work or name

English

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publication date

July 1993

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295-9

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cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

Azorean disease of the nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

Positional cloning: let's not call it reverse anymore

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Dinucleotide repeat polymorphism at the D6S89 locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Dinucleotide repeat polymorphism at the D6S109 locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990).

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

The human gene encoding insulin-like growth factor I is located on chromosome 12.

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Search for the chromosomal location of autosomal dominant cerebellar ataxia from Holguin, Cuba: exclusion from candidate regions on chromosome 4 and 11q

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0793-295

7 January 2021