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Fucheng Li

Showing results (51-60 of 67) with videos related to

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Frontiers in Genetics|September 25, 2023
Exome sequencing improves genetic diagnosis of congenital orofacial cleftsShujuan Yan, Fang Fu, Ru Li, et al.
Frontiers in Genetics|October 3, 2022
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencingFang Fu, Ru Li, Xiao Dang, et al.
The Journal of Pediatrics|May 14, 2016
Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel MutationsFucheng Li, Zhihui Yue, Tingting Xu, et al.
Molecular Cytogenetics|September 28, 2024
Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective studyLu Zhang, Ruibin Huang, Hang Zhou, 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.
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.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 6, 2021
[Application of whole exome sequencing technology in fetuses with congenital structural abnormalities]Lushan Li, Fang Fu, Ru Li, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 14, 2022
Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testingJunhui Wan, Ru Li, Fatao Li, et al.
Human Genetics|March 21, 2015
Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regionsYe Wang, Peiqiang Su, Bin Hu, et al.
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlationsRuibin Huang, Fang Fu, Fei Guo, et al.
Pageof 7

Showing results (51-60 of 67) with videos related to

Sort By:
Pageof 7
Frontiers in Genetics|September 25, 2023
Exome sequencing improves genetic diagnosis of congenital orofacial cleftsShujuan Yan, Fang Fu, Ru Li, et al.
Frontiers in Genetics|October 3, 2022
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencingFang Fu, Ru Li, Xiao Dang, et al.
The Journal of Pediatrics|May 14, 2016
Dent Disease in Chinese Children and Findings from Heterozygous Mothers: Phenotypic Heterogeneity, Fetal Growth, and 10 Novel MutationsFucheng Li, Zhihui Yue, Tingting Xu, et al.
Molecular Cytogenetics|September 28, 2024
Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective studyLu Zhang, Ruibin Huang, Hang Zhou, 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.
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.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 6, 2021
[Application of whole exome sequencing technology in fetuses with congenital structural abnormalities]Lushan Li, Fang Fu, Ru Li, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 14, 2022
Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testingJunhui Wan, Ru Li, Fatao Li, et al.
Human Genetics|March 21, 2015
Characterization of 26 deletion CNVs reveals the frequent occurrence of micro-mutations within the breakpoint-flanking regions and frequent repair of double-strand breaks by templated insertions derived from remote genomic regionsYe Wang, Peiqiang Su, Bin Hu, et al.
American Journal of Obstetrics & Gynecology MFM|November 20, 2023
Prenatal diagnosis of polycystic renal diseases: diagnostic yield, novel disease-causing variants, and genotype-phenotype correlationsRuibin Huang, Fang Fu, Fei Guo, et al.
Pageof 7