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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 22, 2022
[Tandem mass spectrometry and genetic variant analysis of four neonates with very long chain acyl-coenzyme A dehydrogenase deficiency]Dongyang Hong, Yanyun Wang, Yun Sun, et al.Molecular Medicine Reports|January 20, 2016
Genetic counseling for patients with nonsyndromic hearing impairment directed by gene analysisDingyuan Ma, Jingjing Zhang, Chunyu Luo, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 10, 2016
[Mutation screening and prenatal diagnosis of methylmalonic academia in a Chinese pedigree by Ion Torrent semiconductor sequencing]Li Li, Dingyuan Ma, Yun Sun, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|January 31, 2015
[Detection of pathogenic mutations for methylmalonic acidemia using new-generation semiconductor targeted sequencing]Yun Sun, Tao Jiang, Dingyuan Ma, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2018
[Clinical report of testicular hypoplasia combined with 21-hydroxylase deficiency]Bo Jiang, Dingyuan Ma, Huanhuan Chen, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 6, 2024
[Analysis of pathogenicity and genotype-phenotype correlation of the c.158G>A variant of phenylalanine hydroxylase gene]Peiying Yang, Yun Sun, Xin Wang, et al.Journal of Pharmaceutical and Biomedical Analysis|November 5, 2018
A method using angiotensin converting enzyme immobilized on magnetic beads for inhibitor screeningWeiwei Tang, Bingjie Jia, Jie Zhou, et al.Frontiers in Genetics|February 8, 2021
Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese PopulationXin Wang, Yanyun Wang, Dingyuan Ma, et al.Orphanet Journal of Rare Diseases|May 13, 2021
Neonatal screening and genotype-phenotype correlation of hyperphenylalaninemia in the Chinese populationXin Wang, Yanyun Wang, Dingyuan Ma, et al.Gene|March 29, 2023
Identification of two novel DNAJC12 gene variants in a patient with mild hyperphenylalaninemiaLulu Wang, Dingyuan Ma, Yun Sun, et al.Pageof 6