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

Articles > Article · 2009

Authors: P. S. HART, Sema BECERİK, Dilşah ÇOĞULU, Gülnur EMİNGİL, D. Ozdemir-Ozenen, S. T. HAN, P. P. SULIMA, E. Firatli, T. C. HART

Clinical Genetics, Journal Indexed in SCI Expanded, International, WoS, 2009, vol 75, pp 401-404

DOI: 10.1111/j.1399-0004.2008.01112.x

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