Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion (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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published in

Nature Genetics

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volume

6

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issue

2

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page(s)

210-3

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cites work

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Progressive cone-rod degeneration

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Segregation distorters

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Telangiectasia and Optic Atrophy in Cone-Rod Degenerations

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

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Retinal dystrophy and macular coloboma

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Retinal degeneration in hereditary ataxia

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

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

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Rhodopsin mutations in autosomal dominant retinitis pigmentosa.

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

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

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The cone degenerations

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

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Ocular changes in myotonic dystrophy

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A medley of retinal dystrophies

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

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Evidence of founder chromosomes in fragile X syndrome

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

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Strategies for multilocus linkage analysis in humans

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