Showing results (11-20 of 46) with videos related to
Sort By:
Pageof 5
Clinical Genetics|March 8, 2008
Three novel mutations in the PORCN gene underlying focal dermal hypoplasiaP Leoyklang, K Suphapeetiporn, S Wananukul, et al.International Journal of Oral and Maxillofacial Surgery|March 22, 2008
Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palateS Tongkobpetch, K Suphapeetiporn, P Siriwan, et al.Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|November 15, 2000
A cost-benefit of gnRH stimulation test in diagnosis of central precocious puberty (CPP)S Wacharasindhu, S Srivuthana, S Aroonparkmongkol, et al.Clinical Genetics|February 21, 2007
Expanding the phenotypic spectrum of Caffey diseaseK Suphapeetiporn, S Tongkobpetch, A Mahayosnond, et al.Clinical Imaging|July 4, 2001
Subdural empyema secondary to odontogenic masticator space abscess: detection by indium-111-labeled white cell scanV Shotelersuk, M Goyal, J N Rauchenstein, et al.Journal of Endocrinological Investigation|July 29, 2011
Pathogenic mechanism of mutations in the thyroid hormone receptor β geneS Pongjantarasatian, S Wacharasindhu, S Tongkobpetch, et al.Journal of Inherited Metabolic Disease|February 26, 2009
Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine diseaseR Tammachote, S Tongkobpetch, T Desudchit, et al.Clinical Genetics|January 26, 2010
Holocarboxylase synthetase deficiency: novel clinical and molecular findingsR Tammachote, S Janklat, S Tongkobpetch, et al.Genetics and Molecular Research : GMR|March 18, 2016
Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondylo-epiphyseal dysplasia congenitaA Sangsin, C Srichomthong, M Pongpanich, et al.Oral Diseases|March 5, 2017
A novel GJA1 mutation in oculodentodigital dysplasia with extensive loss of enamelT Porntaveetus, C Srichomthong, A Ohazama, et al.Pageof 5