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Expression of Gja1 correlates with the phenotype observed in oculodentodigital syndrome/type III syndactyly

    Research output: Contribution to journal › Article (Academic Journal) › peer-review

    96 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)60-7
    Number of pages8
    JournalJournal of Medical Genetics
    Volume41
    Issue number1
    Publication statusPublished - Jan 2004

    Keywords

    • Abnormalities, Multiple
    • Amino Acid Sequence
    • Animals
    • Cattle
    • Connexin 43
    • Craniofacial Abnormalities
    • Cricetinae
    • Embryo, Mammalian
    • Eye Abnormalities
    • Fingers
    • Gene Expression Regulation, Developmental
    • Humans
    • Mice
    • Molecular Sequence Data
    • Mutation, Missense
    • Phenotype
    • Rats
    • Sequence Alignment
    • Syndactyly
    • Syndrome
    • Tooth Abnormalities

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