Lv1
10 积分 2022-01-18 加入
Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria
9小时前
待确认
Mutation analysis of PAH gene in patients with PKU in western Iran and its association with polymorphisms: identification of four novel mutations
9小时前
待确认
PREVALENCE OF PAH MUTATIONS IN GEORGIAN PKU PATIENTS COMPARED TO MOST FREQUENT PAH MUTATIONS IN EUROPEAN POPULATIONS
10小时前
求助中
Phenylketonuria mutations in Europe
10小时前
已完结
Mutational and phenotypical spectrum of phenylalanine hydroxylase deficiency in Denmark
11小时前
已完结
Phenylketonuria mutations in Germany
11小时前
待确认
Molecular newborn screening of four genetic diseases in Guizhou Province of South China
5天前
已完结
Hyperphenylalaninemia screening in Guangzhou from 2007 to 2016 and gene analysis of 36 phenylalanine hydroxylase deficiency infants
6天前
已完结
Newborn screening and genetic features of patients with hyperphenylalaninemia in a southern Chinese population
6天前
已完结
[Screening of phenylketonuria and analysis of phenylalanine hydroxylase gene in 380 996 newborns from Hainan province]
6天前
已完结
皖公网安备34019202002308
