BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells

by Piranit Nik Kantaputra
Published 2018

Response to the Letter to the Editor by Idil Kurtulus-Waschulewski; Gerhard Wahl, Prof. Dr.; Katalyn Dittrich; Volker Schuster

by Piranit Nik Kantaputra
Published 2018

Clinical Correlate: CLCN7-Associated Autosomal Recessive Osteopetrosis

by Piranit Nik Kantaputra
Published 2018

Clinical Correlate: CLCN7-Associated Autosomal Recessive Osteopetrosis

by Piranit Nik Kantaputra
Published 2018

BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cells

by Piranit Nik Kantaputra
Published 2018

Response to the Letter to the Editor by Idil Kurtulus-Waschulewski; Gerhard Wahl, Prof. Dr.; Katalyn Dittrich; Volker Schuster

by Piranit Nik Kantaputra
Published 2018

Multiple supernumerary molars, anterior openbite, and large ear lobules in mucopolysaccharidosis type VI patient

by Hülya Kayserili, Piranit Nik Kantaputra
Published 2018

Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations

by Onnida Wattanarat, Piranit Nik Kantaputra
Published 2018

Syndromes with supernumerary teeth

by Mark Lubinsky, Piranit Nik Kantaputra
Published 2018

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

by Piranit Nik Kantaputra, Worrachet Intachai, Prim Auychai
Published 2018

Re: Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies [Kantaputra et al. 2004. Am J Med Genet 130A:181-190] [4] (multiple letters)

by Judith G. Hall, Piranit Nik Kantaputra, Pranoot Tanpaiboon
Published 2018

Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: Report of a novel ADAR1 mutation

by Piranit Nik Kantaputra, Wannapa Chinadet, Atsushi Ohazama, Michihiro Kono
Published 2018

Impaired dentin mineralization, supernumerary teeth, hypoplastic mandibular condyles with long condylar necks, and a TRPS1 mutation

by Piranit Nik Kantaputra, Stephanie A. Coury, Wen Hann Tan
Published 2020

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

by Piranit Nik Kantaputra, Worrachet Intachai, Bruce M. Carlson, Chulabhorn Pruksachatkunakorn
Published 2020

Making extra teeth: Lessons from a TRPS1 mutation

by Worawan Kunotai, Panjit Ananpornruedee, Mark Lubinsky, Apitchaya Pruksametanan, Piranit Nik Kantaputra
Published 2018

Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation

by Piranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, Chanin Limwongse
Published 2018

Making extra teeth: Lessons from a TRPS1 mutation

by Worawan Kunotai, Panjit Ananpornruedee, Mark Lubinsky, Apitchaya Pruksametanan, Piranit Nik Kantaputra
Published 2018

Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutation

by Piranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, Chanin Limwongse
Published 2018

Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and aCOL1A2mutation

by Piranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Worrachet Intachai, Chumpol Ngamphiw, Sissades Tongsima, Prapai Dejkhamron
Published 2018

A novel mutation in CDKN1C in sibs with Beckwith-Wiedemann syndrome and cleft palate, sensorineural hearing loss, and supernumerary flexion creases

by Piranit Nik Kantaputra, Rekwan Sittiwangkul, Nuntigar Sonsuwan, Valeria Romanelli, Jair Tenorio, Pablo Lapunzina
Published 2018