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Piranit Nik Kantaputra

Showing results (1-10 of 34) with videos related to

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American Journal of Medical Genetics. Part A|June 3, 2016
Syndromes with supernumerary teethMark Lubinsky, Piranit Nik Kantaputra
American Journal of Medical Genetics. Part A|October 15, 2015
Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutationsOnnida Wattanarat, Piranit Nik Kantaputra
Archives of Oral Biology|May 23, 2020
Impaired dentin mineralization, supernumerary teeth, hypoplastic mandibular condyles with long condylar necks, and a TRPS1 mutationPiranit Nik Kantaputra, Stephanie A Coury, Wen-Hann Tan
American Journal of Medical Genetics. Part A|July 24, 2012
Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: report of a novel ADAR1 mutationPiranit Nik Kantaputra, Wannapa Chinadet, Atsushi Ohazama, et al.
American Journal of Medical Genetics. Part A|October 6, 2016
Making extra teeth: Lessons from a TRPS1 mutationWorawan Kunotai, Panjit Ananpornruedee, Mark Lubinsky, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutationPiranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, et al.
American Journal of Medical Genetics. Part A|December 1, 2012
A 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, et al.
European Journal of Medical Genetics|February 11, 2018
Split hand-foot malformation and a novel WNT10B mutationPiranit Nik Kantaputra, Seema Kapoor, Prashant Verma, et al.
Journal of Human Genetics|April 12, 2018
Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutationPiranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Worrachet Intachai, et al.
European Journal of Medical Genetics|October 5, 2014
Root dentin anomaly and a PLG mutationNapaporn Tananuvat, Pimlak Charoenkwan, Atsushi Ohazama, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|June 3, 2016
Syndromes with supernumerary teethMark Lubinsky, Piranit Nik Kantaputra
American Journal of Medical Genetics. Part A|October 15, 2015
Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutationsOnnida Wattanarat, Piranit Nik Kantaputra
Archives of Oral Biology|May 23, 2020
Impaired dentin mineralization, supernumerary teeth, hypoplastic mandibular condyles with long condylar necks, and a TRPS1 mutationPiranit Nik Kantaputra, Stephanie A Coury, Wen-Hann Tan
American Journal of Medical Genetics. Part A|July 24, 2012
Dyschromatosis symmetrica hereditaria with long hair on the forearms, hypo/hyperpigmented hair, and dental anomalies: report of a novel ADAR1 mutationPiranit Nik Kantaputra, Wannapa Chinadet, Atsushi Ohazama, et al.
American Journal of Medical Genetics. Part A|October 6, 2016
Making extra teeth: Lessons from a TRPS1 mutationWorawan Kunotai, Panjit Ananpornruedee, Mark Lubinsky, et al.
American Journal of Medical Genetics. Part A|June 9, 2012
Severe plexiform facial neurofibromatosis, type 1 with underdeveloped eyes and a novel NF1 mutationPiranit Nik Kantaputra, Ans van den Ouweland, Tumtip Sangruchi, et al.
American Journal of Medical Genetics. Part A|December 1, 2012
A 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, et al.
European Journal of Medical Genetics|February 11, 2018
Split hand-foot malformation and a novel WNT10B mutationPiranit Nik Kantaputra, Seema Kapoor, Prashant Verma, et al.
Journal of Human Genetics|April 12, 2018
Osteogenesis imperfecta with ectopic mineralizations in dentin and cementum and a COL1A2 mutationPiranit Nik Kantaputra, Yuddhasert Sirirungruangsarn, Worrachet Intachai, et al.
European Journal of Medical Genetics|October 5, 2014
Root dentin anomaly and a PLG mutationNapaporn Tananuvat, Pimlak Charoenkwan, Atsushi Ohazama, et al.
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