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Yanling Teng

Showing results (31-40 of 38) with videos related to

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QJM : Monthly Journal of the Association of Physicians|February 21, 2025
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencingHongyun Zhang, Jun He, Yanling Teng, et al.
Molecular Genetics & Genomic Medicine|July 22, 2021
Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and reviewJing Liu, Qin Liu, Shuting Yang, et al.
Human Genetics|January 4, 2021
Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosisXin Chen, Wu Yin, Siyi Chen, et al.
Frontiers in Genetics|July 24, 2023
Functional identification of two novel variants and a hypomorphic variant in <i>ASS1</i> from patients with Citrullinemia type IJing Liu, Zhongjie Wang, Huiming Yan, et al.
Cell Reports|November 19, 2023
A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorderHanzhe Kuang, Yunlong Li, Yixuan Wang, et al.
Journal of Neurophysiology|January 17, 2024
Motor patterns of patients with spinal muscular atrophy suggestive of sensory and corticospinal contributions to the development of locomotor muscle synergiesVincent C K Cheung, Sophia C W Ha, Janet H Zhang-Lea, et al.
Thrombosis Research|July 30, 2025
Variant analysis of F8 in 123 patients with hemophilia A: Identification of 18 novel variantsYanling Teng, Wen Zhang, Huimin Zhu, et al.
The Journal of Molecular Diagnostics : JMD|July 22, 2021
A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA)Qiaowei Liang, Wanqian Gu, Ping Chen, et al.
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Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
QJM : Monthly Journal of the Association of Physicians|February 21, 2025
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencingHongyun Zhang, Jun He, Yanling Teng, et al.
Molecular Genetics & Genomic Medicine|July 22, 2021
Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and reviewJing Liu, Qin Liu, Shuting Yang, et al.
Human Genetics|January 4, 2021
Loss of PIGK function causes severe infantile encephalopathy and extensive neuronal apoptosisXin Chen, Wu Yin, Siyi Chen, et al.
Frontiers in Genetics|July 24, 2023
Functional identification of two novel variants and a hypomorphic variant in <i>ASS1</i> from patients with Citrullinemia type IJing Liu, Zhongjie Wang, Huiming Yan, et al.
Cell Reports|November 19, 2023
A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorderHanzhe Kuang, Yunlong Li, Yixuan Wang, et al.
Journal of Neurophysiology|January 17, 2024
Motor patterns of patients with spinal muscular atrophy suggestive of sensory and corticospinal contributions to the development of locomotor muscle synergiesVincent C K Cheung, Sophia C W Ha, Janet H Zhang-Lea, et al.
Thrombosis Research|July 30, 2025
Variant analysis of F8 in 123 patients with hemophilia A: Identification of 18 novel variantsYanling Teng, Wen Zhang, Huimin Zhu, et al.
The Journal of Molecular Diagnostics : JMD|July 22, 2021
A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA)Qiaowei Liang, Wanqian Gu, Ping Chen, et al.
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