Microsatellite markers for the cone-rod retinal dystrophy gene, CRX, on 19q13.3 [2]

J. Bellingham, C. Gregory-Evans

    Research output: Contribution to journalArticlepeer-review

    Original languageEnglish
    Pages (from-to)527
    JournalJournal of Medical Genetics
    Volume35
    Issue number6
    Publication statusPublished - 1998

    Keywords

    • Chromosome Mapping
    • Chromosomes, Human, Pair 19
    • Cones (Retina)
    • Genes, Homeobox
    • Genetic Markers
    • Heterozygote Detection
    • Humans
    • Microsatellite Repeats
    • Molecular Sequence Data
    • Polymorphism, Genetic
    • genetics: Retinal Degeneration
    • Rods (Retina)

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