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Dento Maxillo Facial Radiology|January 30, 2009
Bilateral submandibular gland aplasia with clinico-radiological mass due to prolapsing sublingual salivary tissue through mylohyoid boutonniere: a case report and reviewM Ahmed, M Strauss, A Kassaie, et al.Genetics and Molecular Research : GMR|November 5, 2015
Pyridoxal 5ꞌ-phosphate-responsive epilepsy with novel mutations in the PNPO gene: a case reportM Veeravigrom, P Damrongphol, R Ittiwut, et al.The Southeast Asian Journal of Tropical Medicine and Public Health|September 15, 2001
A case of Pfeiffer syndrome type 1 with an A344P mutation in the FGFR2 geneV Shotelersuk, S Srivuthana, C Ittiwut, et al.Oral Diseases|November 10, 2017
A novel PITX2 mutation in non-syndromic orodental anomaliesN Intarak, T Theerapanon, C Ittiwut, et al.Oncology Reports|October 18, 2001
Fibroblast growth factor receptor 3 S249C mutation in virus associated squamous cell carcinomasV Shotelersuk, C Ittiwut, K Shotelersuk, et al.Genetics and Molecular Research : GMR|October 6, 2016
Novel mutations in the FUCA1 gene that cause fucosidosisW Panmontha, P Amarinthnukrowh, P Damrongphol, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|July 9, 2004
Pallister-Hall syndrome with hypoparathyroidismS Wacharasindhu, V Shotelersuk, S Srivuthana, et al.American Journal of Medical Genetics|September 14, 1999
Discordance of oral-facial-digital syndrome type 1 in monozygotic twin girlsV Shotelersuk, C J Tifft, S Vacha, et al.Chest|January 13, 2000
Pulmonary function and high-resolution CT findings in patients with an inherited form of pulmonary fibrosis, Hermansky-Pudlak syndrome, due to mutations in HPS-1M Brantly, N A Avila, V Shotelersuk, et al.Oral Diseases|November 9, 2017
Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutationT Porntaveetus, T Osathanon, N Nowwarote, et al.Pageof 5