(Q28252272)

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A Fryer

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C Inglehearn

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J Duvall-Young

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J L Whittaker

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C Y Gregory

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R Butler

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N Ebenezer

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D M Hunt

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S Bhattacharya

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

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language of work or name

English

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publication date

February 1994

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210-3

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0294-210

Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13

21 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0294-210

Progressive cone-rod degeneration

21 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

A second-generation linkage map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

21 January 2018

Segregation distorters

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

Cone and cone-rod dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Telangiectasia and Optic Atrophy in Cone-Rod Degenerations

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Progressive cone-rod dystrophy and high myopia in a Finnish family

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Retinal dystrophy and macular coloboma

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Retinal degeneration in hereditary ataxia

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

A progressive cone-rod dystrophy and amelogenesis imperfecta: a new syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Autosomal dominant cone-rod dystrophy: a linkage study with 17 biochemical and serological markers

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

The cone degenerations

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q.

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Ocular changes in myotonic dystrophy

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

A medley of retinal dystrophies

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Evidence of founder chromosomes in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

A computer program to make linkage analysis with LIPED and LINKAGE easier to perform and less prone to input errors

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0294-210

7 January 2021