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Browsing by Author Piranit Nik Kantaputra

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Showing results 15 to 34 of 37 < previous   next >
Issue DateTitleAuthor(s)
1-Nov-2020Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2Piranit Nik Kantaputra; Prapai Dejkhamron; Sissades Tongsima; Chumpol Ngamphiw; Worrachet Intachai; Lukana Ngiwsara; Phannee Sawangareetrakul; Jisnuson Svasti; Bjorn Olsen; James R.Ketudat Cairns; Kanokkan Bumroongkit
1-Feb-2021Juberg-Hayward syndrome is a cohesinopathy, caused by mutation in ESCO2Piranit Nik Kantaputra; Prapai Dejkhamron; Worrachet Intachai; Chumpol Ngamphiw; Katsushige Kawasaki; Atsushi Ohazama; Suttichai Krisanaprakornkit; Bjorn Olsen; Sissades Tongsima; Jame R. Ketudat Cairns
1-Jan-2017Making extra teeth: Lessons from a TRPS1 mutationWorawan Kunotai; Panjit Ananpornruedee; Mark Lubinsky; Apitchaya Pruksametanan; Piranit Nik Kantaputra
1-Jul-2012Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patientHülya Kayserili; Piranit Nik Kantaputra
1-Oct-2022Mutations in LRP5 and BMP4 are associated with mesiodens, tooth agenesis, root malformation, and oral exostosesPiranit Nik Kantaputra; Yeliz Guven; Kanich Tripuwabhrut; Ploy Adisornkanj; Athiwat Hatsadaloi; Massupa Kaewgahya; Bjorn Olsen; Chumpol Ngamphiw; Peeranat Jatooratthawichot; Sissades Tongsima; James R. Ketudat Cairns
1-Jan-2013A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creasesPiranit Nik Kantaputra; Rekwan Sittiwangkul; Nuntigar Sonsuwan; Valeria Romanelli; Jair Tenorio; Pablo Lapunzina
1-Dec-2021A novel P3H1 mutation is associated with osteogenesis imperfecta type VIII and dental anomaliesPiranit Nik Kantaputra; Prapai Dejkhamron; Worrachet Intachai; Chumpol Ngamphiw; James R. Ketudat Cairns; Katsushige Kawasaki; Atsushi Ohazama; Bjorn Olsen; Sissades Tongsima; Salita Angkurawaranon
1-Jan-2014Oral manifestations of 17 patients affected with mucopolysaccharidosis type VIPiranit Nik Kantaputra; Hülya Kayserili; Yeliz Güven; Warissara Kantaputra; Mehmet C. Balci; Pranoot Tanpaiboon; Anusha Uttarilli; Ashwin Dalal
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-2017Periodontal disease and FAM20A mutationsPiranit Nik Kantaputra; Chotika Bongkochwilawan; Mark Lubinsky; Supansa Pata; Massupa Kaewgahya; Huei Jinn Tong; James R. Ketudat Cairns; Yeliz Guven; Nipon Chaisrisookumporn
1-Jan-2016Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutationsOnnida Wattanarat; Piranit Nik Kantaputra
15-May-2005Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190] [4] (multiple letters)Judith G. Hall; Piranit Nik Kantaputra; Pranoot Tanpaiboon
1-Jan-2015Response to the Letter to the Editor by Idil Kurtulus-Waschulewski; Gerhard Wahl, Prof. Dr.; Katalyn Dittrich; Volker SchusterPiranit Nik Kantaputra
1-Jan-2014Root dentin anomaly and a PLG mutationNapaporn Tananuvat; Pimlak Charoenkwan; Atsushi Ohazama; James R. Ketuda Cairns; Massupa Kaewgahya; Piranit Nik Kantaputra
1-Jul-2012Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutationPiranit Nik Kantaputra; Ans van den Ouweland; Tumtip Sangruchi; Chanin Limwongse
1-Jul-2018Split hand-foot malformation and a novel WNT10B mutationPiranit Nik Kantaputra; Seema Kapoor; Prashant Verma; Worrachet Intachai; James R. Ketudat Cairns
1-Oct-2016Syndromes with supernumerary teethMark Lubinsky; Piranit Nik Kantaputra
1-Aug-2017TFAP2B mutation and dental anomaliesNatchaya Tanasubsinn; Rekwan Sittiwangkul; Yupada Pongprot; Katsushige Kawasaki; Atsushi Ohazama; Thanapat Sastraruji; Massupa Kaewgahya; Piranit Nik Kantaputra
1-Sep-2020Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapesPiranit Nik Kantaputra; Kanich Tripuwabhrut; Worrachet Intachai; Bruce M. Carlson; Natalina Quarto; Chumpol Ngamphiw; Sissades Tongsima; Nuntigar Sonsuwan
1-Jul-2020TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphologyPiranit Nik Kantaputra; Dhirawat Jotikasthira; Bruce Carlson; Teerapat Wongmaneerung; Natalina Quarto; Theerapong Khankasikum; Warit Powcharoen; Worrachet Intachai; Kanich Tripuwabhrut
Showing results 15 to 34 of 37 < previous   next >