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First Case Report of EX3del4765 Mutation in PAH Gene in Asian Population
Gene Deletion Phenylalanine Hydroxylase Phenylketonuria
2016/1/26
Introduction: Phenylketonuria (PKU) is an autosomal recessive inborn error of phenylalanine metabolism, which is caused by mutation in phenylalanine hydroxylase (PAH) gene. Most of the PAH mutations a...
SUPERNUMERARY NIPPLE:First case report in Iran
SUPERNUMERARY NIPPLE First case report Iran
2009/12/7
SUPERNUMERARY NIPPLE:First case report in Iran。