Lv41
720 积分 2022-12-15 加入
甲醛通过调节BDNF通路降低ICR小鼠学习记忆功能
1个月前
已完结
Detection of CPS1 gene mutation in a neonate with carbamoyl phosphate synthetase I deficiency
11个月前
已完结
[Analysis of newborn screening for galactosemia and genotype-phenotype of confirmed galatosemia cases]
1年前
已完结
Diagnosis of two neonates with galactosemia by using next generation sequencing
1年前
已完结
Molecular and biochemical basis for variants and deficiency of GALT: report of 4 novel mutations
1年前
已关闭
Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes Project*
1年前
已完结
Identification of two novel DNAJC12 gene variants in a patient with mild hyperphenylalaninemia
1年前
已完结
Clinical and molecular characterization of 10 Chinese children with congenital adrenal hyperplasia due to 11beta-hydroxylase deficiency
1年前
已完结
Newborn screening of maple syrup urine disease and the effect of early diagnosis
1年前
已完结
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