Browsing by Author Piranit Kantaputra

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Showing results 1 to 10 of 10
Issue DateTitleAuthor(s)
1-Jan-2020Clouston syndrome with pili canaliculi, pili torti, overgrown hyponychium, onycholysis, taurodontism and absence of palmoplantar keratodermaPiranit Kantaputra; Worrachet Intachai; Katsushige Kawasaki; Atsushi Ohazama; Bruce Carlson; Natalina Quarto; Chulabhorn Pruksachatkun; Mati Chuamanochan
1-Jan-2022Expanding genotypic and phenotypic spectrums of LTBP3 variants in dental anomalies and short stature syndromePiranit 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
1-Aug-2009Expanding the phenotypic spectrum of acro-cardio-facial syndrome (ACFS): Exclusion of P63 mutationPranoot Tanpaiboon; Rekwan Sittiwangkul; Prapai Dejkhamron; Metawee Srikummool; Warissara Sripathomsawat; Piranit Kantaputra
1-Jan-2020Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantationNapaporn Tananuvat; Rak Tananuvat; Wattana Chartapisak; Pongsak Mahanupab; Chananya Hokierti; Metawee Srikummool; Jatupol Kampuansai; Worrachet Intachai; Bjorn Olsen; James R. Ketudat Cairns; Piranit Kantaputra
1-Jan-2022Novel Dental Anomaly–associated Mutations in WNT10A Protein Binding SitesPiranit Kantaputra; Peeranat Jatooratthawichot; Oranuch Tantachamroon; Kamonporn Nanekrungsan; Worrachet Intachai; Bjorn Olsen; Sissades Tongsima; Chumpol Ngamphiw; James R.Ketudat Cairns
1-Jan-2011Phenotypic analysis of Arg227 mutations of TP63 with emphasis on dental phenotype and micturition difficulties in EEC syndromeWarissara Sripathomsawat; Pranoot Tanpaiboon; Jan Heering; Volker Dötsch; Raoul C M Hennekam; Piranit Kantaputra
1-Jun-2011The smallest teeth in the world are caused by mutations in the PCNT genePiranit Kantaputra; Pranoot Tanpaiboon; Thantrira Porntaveetus; Atsushi Ohazama; Paul Sharpe; Anita Rauch; Atiwat Hussadaloy; Christian T. Thiel
1-Jan-2012TBX22 mutation associated with cleft lip/palate, hypodontia, and limb anomalyArunee Kaewkhampa; Dhirawat Jotikasthira; Sutti Malaivijitnond; Piranit Kantaputra
1-May-2011WNT10A and isolated hypodontiaPiranit Kantaputra; Warissara Sripathomsawat
1-May-2022WNT10A variant and severe scoliosis?Piranit Kantaputra; Bjorn Olsen; John A. McGrath