Hereditary retinopathies: insights into a complex genetic aetiology.

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Hereditary retinopathies: insights into a complex genetic aetiology.

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1993 nî lūn-bûn

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1993年の論文

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1993年学术文章

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1993年学术文章

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1993年学术文章

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1993年学术文章

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1993年学术文章

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1993年學術文章

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1993年學術文章

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1993年學術文章

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Hereditary retinopathies: insights into a complex genetic aetiology.

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Hereditary retinopathies: insights into a complex genetic aetiology.

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Hereditary retinopathies: insights into a complex genetic aetiology.

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Hereditary retinopathies: insights into a complex genetic aetiology.

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Hereditary retinopathies: insights into a complex genetic aetiology.

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Hereditary retinopathies: insights into a complex genetic aetiology.

@nl

P1476

Hereditary retinopathies: insights into a complex genetic aetiology.

@en

P2093

Humphries P

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P2860

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests

Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene

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

Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase.

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa.

A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p.

Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.

P304

469-470

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P31

scholarly article

editorial

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10.1136/BJO.77.8.469

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P407

English

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P478

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P577

1993-08-01T00:00:00Z

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15174286

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P698

8025039

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504576

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