1. CMU Intellectual Repository

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Results 1-10 of 23 (Search time: 0.002 seconds).
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Issue DateTitleAuthor(s)
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-Jan-2014Twins with hereditary sensory and autonomic neuropathy type IV with preserved periodontal sensationYeliz Guven; Umut Altunoglu; Oya Aktoren; Zehra Oya Uyguner; Hulya Kayserili; Massupa Kaewkahya; Piranit 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-Jan-2014Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutationPiranit Nik Kantaputra; Chotika Bongkochwilawan; Massupa Kaewgahya; Atsushi Ohazama; Hulya Kayserili; Arzu Pinar Erdem; Oya Aktoren; Yeliz Guven
1-Jan-2014Enamel-renal-gingival syndrome and FAM20A mutationsPiranit Nik Kantaputra; Massupa Kaewgahya; Udomrat Khemaleelakul; Prapai Dejkhamron; Suchitra Sutthimethakorn; Visith Thongboonkerd; Anak Iamaroon
1-Jan-2014BCOR mutations and unstoppable root growth: A commentary on oculofaciocardiodental syndrome: Novel BCOR mutations and expression in dental cellsPiranit Nik Kantaputra
1-Jan-2014Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutationsPiranit Nik Kantaputra; Hulya Kayserili; Yeliz Guven; Warissara Kantaputra; Mehmet C. Balci; Pranoot Tanpaiboon; Napaporn Tananuvat; Anusha Uttarilli; Ashwin Dalal
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-Sep-2012Dyschromatosis 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; Michihiro Kono
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

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