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Fengxia Yao

Showing results (21-30 of 34) with videos related to

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Frontiers in Genetics|January 30, 2023
Phenotypic and genetic characteristics of 130 patients with mucopolysaccharidosis type II: A single-center retrospective study in ChinaZhenjie Zhang, Mingsheng Ma, Weimin Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 3, 2014
[The mutation analysis of PAH gene and prenatal diagnosis in classical phenylketonuria family]Yousheng Yan, Shengju Hao, Fengxia Yao, et al.
Human Genomics|November 28, 2024
Long-read sequencing enables comprehensive molecular genetic diagnosis of Fabry diseaseFengxia Yao, Na Hao, Danhua Li, et al.
Journal of Inherited Metabolic Disease|June 24, 2025
Long-Read Sequencing Expands the Genotypic Spectrum of Patients With Mucopolysaccharidosis Type IINa Hao, Fengxia Yao, Danhua Li, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 16, 2023
Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathyHuajin Li, Xing Wei, Shijing Wu, et al.
Molecular Vision|May 20, 2021
Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7Xuan Zou, Fengxia Yao, Fengrong Li, et al.
Molecular Cytogenetics|July 17, 2012
Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortionJinsong Gao, Congcong Liu, Fengxia Yao, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 2024
Approach to the Patient: Diagnosis and Treatment With Growth Hormone of Turner Syndrome and Its VariantsZhibo Zhou, Jiaqi Qiang, Na Hao, et al.
Prenatal Diagnosis|April 17, 2016
Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluidQingwei Qi, Sijia Lu, Xiya Zhou, et al.
Human Mutation|November 10, 2019
Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophiesChao Ling, Yi Dai, Li Fang, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Frontiers in Genetics|January 30, 2023
Phenotypic and genetic characteristics of 130 patients with mucopolysaccharidosis type II: A single-center retrospective study in ChinaZhenjie Zhang, Mingsheng Ma, Weimin Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 3, 2014
[The mutation analysis of PAH gene and prenatal diagnosis in classical phenylketonuria family]Yousheng Yan, Shengju Hao, Fengxia Yao, et al.
Human Genomics|November 28, 2024
Long-read sequencing enables comprehensive molecular genetic diagnosis of Fabry diseaseFengxia Yao, Na Hao, Danhua Li, et al.
Journal of Inherited Metabolic Disease|June 24, 2025
Long-Read Sequencing Expands the Genotypic Spectrum of Patients With Mucopolysaccharidosis Type IINa Hao, Fengxia Yao, Danhua Li, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 16, 2023
Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathyHuajin Li, Xing Wei, Shijing Wu, et al.
Molecular Vision|May 20, 2021
Clinical characterization and the improved molecular diagnosis of autosomal dominant cone-rod dystrophy in patients with SCA7Xuan Zou, Fengxia Yao, Fengrong Li, et al.
Molecular Cytogenetics|July 17, 2012
Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortionJinsong Gao, Congcong Liu, Fengxia Yao, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 2024
Approach to the Patient: Diagnosis and Treatment With Growth Hormone of Turner Syndrome and Its VariantsZhibo Zhou, Jiaqi Qiang, Na Hao, et al.
Prenatal Diagnosis|April 17, 2016
Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluidQingwei Qi, Sijia Lu, Xiya Zhou, et al.
Human Mutation|November 10, 2019
Exonic rearrangements in DMD in Chinese Han individuals affected with Duchenne and Becker muscular dystrophiesChao Ling, Yi Dai, Li Fang, et al.
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