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Mostrar 1 - 20 resultats de 64 per cerca '(( l narr computers a non ) OR ((( c daily compared less now ) OR ( j can companies can ngoc ))))', hora de la petició: 2.79sec Refinar resultats
AB129. Osteogenesis imperfecta: clinical features and bisphosphonate treatment outcome
AB070. Mutations of SRD5A2 in Vietnamese patients: phenotype and genotype

AB072. Novel mutation in the hepatocyte nuclear factor 1b/maturity-onset diabetes of the young type 5 gene—unreported Vietnamese case
AB073. Mutations in the type II 3β-hydroxysteroid dehydrogenase gene caused primary adrenal insufficiency & 46,XY disorders of sex development

AB132. Neonatal diabetes in Wolcott-Rallison syndrome: a case report
AB124. Mucolipidosis type II: clinical features and laboratories

AB126. Enzyme replacement therapy in patient with mucopolysaccharidosis type I: a case report
AB127. Enzyme replacement therapy in patient with mucopolysaccharidosis type II: a case report

AB102. Vietnamese patient with Tyrosinemia type 1: a case report
AB101. Neonatal form of Isovaleric acidemia in Vietnamese patients: clinical history and outcomes

AB155. Clinical presentation and its relationship with chromosomal abnormalities in Turner syndrome
AB130. Pseudoaldosteronism due to mutation of SCNN1A gene: a case report

AB100. Phenotypes of primary hyperlipidemia in a Vietnamese referral center
AB099. Beta ketothiolase deficiency: phenotype and genotype in Vietnam population

AB078. Novel mutation of ABCC8 and KCNJ11 of children with congenital hyperinsulinism
AB077. Clinical symptoms, molecular genetics, genotype and phenotype correlations of children with congenital hyperinsulinism

AB076. Congenital hyperinsulinism due to mutation of HNF4A: a case report
AB071. Mutations of AR gene in Vietnamese patients: genotype and phenotype

AB131. Genotype, phenotype of transient neonatal diabetes mellitus
AB125. Neonatal diabetes mellitus due to insulin gene mutation

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