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

R Richardson, D Donnai, F Meire, M J Dixon

Research output: Contribution to journalArticle (Academic Journal)peer-review

86 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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