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Frontiers in Endocrinology|March 13, 2023
Association between aberrant amino acid metabolism and nonchromosomal modifications fetal structural anomalies: A cohort studyHuizhen Yuan, Chang Liu, Xinrong Wang, et al.
Frontiers in Genetics|February 27, 2023
Screening and mutation analysis of phenylalanine hydroxylase deficiency in newborns from Jiangxi provinceBaitao Zeng, Qing Lu, Shaohong Chen, et al.
Nature Communications|December 15, 2025
Reconstituting transcription-translation-coupled DNA replication within complex in vitro biological systemsXiao Zheng, Wenli Gao, Wan-Qiu Liu, et al.
Frontiers in Medicine|August 20, 2025
Application of family whole-exome sequencing for prenatal diagnosis-an analysis of 357 casesYijun Ge, Huizhen Yuan, Yao Yu, et al.
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