All enamel is not created equal: Supports from a novel FAM83H mutation

بواسطة Piranit Nik Kantaputra, Worrachet Intachai, Prim Auychai
منشور في 2018

Clouston syndrome with dental anomalies, micropores of hair shafts and absence of palmoplantar keratoderma

بواسطة Piranit Nik Kantaputra, Worrachet Intachai, Bruce M. Carlson, Chulabhorn Pruksachatkunakorn
منشور في 2020

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and aCOL1A2mutation

بواسطة Piranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Worrachet Intachai, Chumpol Ngamphiw, Sissades Tongsima, Prapai Dejkhamron
منشور في 2018

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutation

بواسطة Piranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Worrachet Intachai, Chumpol Ngamphiw, Sissades Tongsima, Prapai Dejkhamron
منشور في 2018

Split hand-foot malformation and a novel WNT10B mutation

بواسطة Piranit Nik Kantaputra, Seema Kapoor, Prashant Verma, Worrachet Intachai, James R. Ketudat Cairns
منشور في 2018

Isolated dentinogenesis imperfecta with glass-like enamel caused by COL1A2 mutation

بواسطة Piranit Nik Kantaputra, Wannapa Chinadet, Worrachet Intachai, Chumpol Ngamphiw, James R. Ketudat Cairns, Sissades Tongsima
منشور في 2018

Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratoderma

بواسطة Piranit Kantaputra, Worrachet Intachai, Katsushige Kawasaki, Atsushi Ohazama, Bruce Carlson, Natalina Quarto, Chulabhorn Pruksachatkun, Mati Chuamanochan
منشور في 2020

Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes

بواسطة Piranit Nik Kantaputra, Kanich Tripuwabhrut, Worrachet Intachai, Bruce M. Carlson, Natalina Quarto, Chumpol Ngamphiw, Sissades Tongsima, Nuntigar Sonsuwan
منشور في 2020

TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morpho...

بواسطة Piranit Nik Kantaputra, Dhirawat Jotikasthira, Bruce Carlson, Teerapat Wongmaneerung, Natalina Quarto, Theerapong Khankasikum, Warit Powcharoen, Worrachet Intachai, Kanich Tripuwabhrut
منشور في 2020

WNT1-associated osteogenesis imperfecta with atrophic frontal lobes and arachnoid cysts

بواسطة Piranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Pannee Visrutaratna, Sasitorn Petcharunpaisan, Bruce M. Carlson, Worrachet Intachai, Jutamas Sudasna, Jatupol Kampuansai, Prapai Dejkhamron
منشور في 2019

Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation

بواسطة Napaporn Tananuvat, Rak Tananuvat, Wattana Chartapisak, Pongsak Mahanupab, Chananya Hokierti, Metawee Srikummool, Jatupol Kampuansai, Worrachet Intachai, Bjorn Olsen, James R. Ketudat Cairns, Piranit Kantaputra
منشور في 2020

ADAMTSL1 and mandibular prognathism

بواسطة Piranit N. Kantaputra, Apitchaya Pruksametanan, Nattapol Phondee, Athiwat Hutsadaloi, Worrachet Intachai, Katsushig Kawasaki, Atsushi Ohazama, Chumpol Ngamphiw, Sissades Tongsima, James R. Ketudat Cairns, Polbhat Tripuwabhrut
منشور في 2019

Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2

بواسطة Piranit Nik Kantaputra, Prapai Dejkhamron, Sissades Tongsima, Chumpol Ngamphiw, Worrachet Intachai, Lukana Ngiwsara, Phannee Sawangareetrakul, Jisnuson Svasti, Bjorn Olsen, James R.Ketudat Cairns, Kanokkan Bumroongkit
منشور في 2020

Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndrome

بواسطة Piranit Kantaputra, Yeliz Guven, Tugba Kalayci, Pelin Karaca Özer, Wannakamon Panyarak, Worrachet Intachai, Bjorn Olsen, Bruce M. Carlson, Oranud Praditsap, Sissades Tongsima, Chumpol Ngamphiw, Peeranat Jatooratthawichot, Abigail S. Tucker, James R. Ketudat Cairns
منشور في 2022