9 results on '"Tongkobpetch S"'
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2. Holocarboxylase synthetase deficiency: novel clinical and molecular findings
3. Prenatal diagnosis of a novel mutation, c.529C>T (p.Q177X), in the BCKDHA gene in a family with maple syrup urine disease
4. Clinical and Molecular Characteristics of Thai Families with Autosomal Recessive Chronic Granulomatous Disease
5. Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate
6. TBX22 mutations are a frequent cause of non-syndromic cleft palate in the Thai population
7. Expanding the phenotypic spectrum of Caffey disease
8. Two novel frameshift mutations of the EBP gene in two unrelated Thai girls with Conradi-Hunermann-Happle syndrome.
9. De novo missense mutation, S541Y, in the p63 gene underlying Rapp-Hodgkin ectodermal dysplasia syndrome
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