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Can Liao

Showing results (231-240 of 262) with videos related to

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Gene|June 11, 2014
Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 regionFang Fu, Huan-ling Liu, Ru Li, et al.
Medicine|December 23, 2022
Intervention of Compound Xueshuantong Capsule on the incidence of heart failure in patients with acute myocardial infarction after PCI based on the combination of disease and syndrome: A multi-center, randomized, double-blind, controlled trialXiao-Dan Yang, Jia-Xi Shi, Wei-Can Liao, et al.
Biomedicines|June 28, 2023
A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal UltrasoundJiajie Tang, Jin Han, Jiaxin Xue, et al.
Acta Obstetricia Et Gynecologica Scandinavica|December 16, 2025
Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine-year retrospective study from ChinaJianqin Lu, Fang Fu, Fei Guo, et al.
BMC Medical Genomics|April 22, 2024
Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygromaFang Fu, Xin Yang, Ru Li, et al.
Genes|December 23, 2022
The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective StudyFang Fu, Ru Li, Qiu-Xia Yu, et al.
American Journal of Translational Research|February 10, 2018
NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathwayFang Fu, Yan Li, Ru Li, et al.
Heliyon|September 17, 2024
Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature reviewRuibin Huang, Chunling Ma, Huanyi Chen, et al.
Human Genetics|April 24, 2023
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingRuibin Huang, Fang Fu, Hang Zhou, et al.
Prenatal Diagnosis|February 16, 2005
Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospitalCan Liao, Qiu-Hua Mo, Jian Li, et al.
Pageof 27

Showing results (231-240 of 262) with videos related to

Sort By:
Pageof 27
Gene|June 11, 2014
Prenatal diagnosis of foetuses with congenital abnormalities and duplication of the MECP2 regionFang Fu, Huan-ling Liu, Ru Li, et al.
Medicine|December 23, 2022
Intervention of Compound Xueshuantong Capsule on the incidence of heart failure in patients with acute myocardial infarction after PCI based on the combination of disease and syndrome: A multi-center, randomized, double-blind, controlled trialXiao-Dan Yang, Jia-Xi Shi, Wei-Can Liao, et al.
Biomedicines|June 28, 2023
A Deep-Learning-Based Method Can Detect Both Common and Rare Genetic Disorders in Fetal UltrasoundJiajie Tang, Jin Han, Jiaxin Xue, et al.
Acta Obstetricia Et Gynecologica Scandinavica|December 16, 2025
Prenatal diagnosis and perinatal outcomes of fetuses with congenital duodenal obstruction: A nine-year retrospective study from ChinaJianqin Lu, Fang Fu, Fei Guo, et al.
BMC Medical Genomics|April 22, 2024
Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygromaFang Fu, Xin Yang, Ru Li, et al.
Genes|December 23, 2022
The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective StudyFang Fu, Ru Li, Qiu-Xia Yu, et al.
American Journal of Translational Research|February 10, 2018
NDUFA4 enhances neuron growth by triggering growth factors and inhibiting neuron apoptosis through Bcl-2 and cytochrome C mediated signaling pathwayFang Fu, Yan Li, Ru Li, et al.
Heliyon|September 17, 2024
Prenatal diagnosis of 17q12 copy number variants in fetuses via chromosomal microarray analysis - A retrospective cohort study and literature reviewRuibin Huang, Chunling Ma, Huanyi Chen, et al.
Human Genetics|April 24, 2023
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingRuibin Huang, Fang Fu, Hang Zhou, et al.
Prenatal Diagnosis|February 16, 2005
Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospitalCan Liao, Qiu-Hua Mo, Jian Li, et al.
Pageof 27