Browsing by Author Worrachet Intachai

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Showing results 3 to 8 of 8 < previous 
Issue DateTitleAuthor(s)
1-Mar-2020Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratodermaPiranit Nik Kantaputra; Worrachet Intachai; Bruce M. Carlson; Chulabhorn Pruksachatkunakorn
1-Jan-2020Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratodermaPiranit Kantaputra; Worrachet Intachai; Katsushige Kawasaki; Atsushi Ohazama; Bruce Carlson; Natalina Quarto; Chulabhorn Pruksachatkun; Mati Chuamanochan
1-Jan-2018Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutationPiranit Nik Kantaputra; Wannapa Chinadet; Worrachet Intachai; Chumpol Ngamphiw; James R. Ketudat Cairns; Sissades Tongsima
1-Jul-2018Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutationPiranit Nik Kantaputra; Yuddhasert Sirirungruangsarn; Worrachet Intachai; Chumpol Ngamphiw; Sissades Tongsima; Prapai Dejkhamron
1-Jul-2018Split hand-foot malformation and a novel WNT10B mutationPiranit Nik Kantaputra; Seema Kapoor; Prashant Verma; Worrachet Intachai; James R. Ketudat Cairns
1-Apr-2019WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cystsPiranit Nik Kantaputra; Yuddhasert Sirirungruangsarn; Pannee Visrutaratna; Sasitorn Petcharunpaisan; Bruce M. Carlson; Worrachet Intachai; Jutamas Sudasna; Jatupol Kampuansai; Prapai Dejkhamron