Deletion of the first pair of fibronectin type III repeats of the integrin β-4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients

Ramon Y. Birnbaum, Daniella Landau, Khalil Elbedour, Rivka Ofir, Ohad S. Birk, Rivka Carmi

Research output: Contribution to journalLetterpeer-review

22 Scopus citations
Original languageEnglish
Pages (from-to)1063-1066
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Issue number8
StatePublished - 15 Apr 2008

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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