Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

HART P. S. , BECERİK S., ÇOĞULU D., EMİNGİL G., Ozdemir-Ozenen D., HAN S. T. , ...More

CLINICAL GENETICS, vol.75, no.4, pp.401-404, 2009 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Letter
  • Volume: 75 Issue: 4
  • Publication Date: 2009
  • Doi Number: 10.1111/j.1399-0004.2008.01112.x
  • Title of Journal : CLINICAL GENETICS
  • Page Numbers: pp.401-404