Homozygous null mutations of ROR2 tyrosine kinase cause the autosomal recessive form of Robinow syndrome.

Brunner H., Celli J., Kayserili H., van Beusekom E., Brussel W., Skovby F., ...More

AMERICAN JOURNAL OF HUMAN GENETICS, vol.67, no.4, pp.40, 2000 (SCI-Expanded, Scopus)

  • Publication Type: Article / Abstract
  • Volume: 67 Issue: 4
  • Publication Date: 2000
  • Journal Name: AMERICAN JOURNAL OF HUMAN GENETICS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.40
  • Gazi University Affiliated: No