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Shanling Liu

Showing results (71-80 of 175) with videos related to

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Prenatal Diagnosis|November 4, 2025
Microcephaly, Cerebellar Hypoplasia, Enlarged Posterior Fossa and Polyhydramnios: Prenatal Phenotypes for CASK-Related DisordersJing Chen, Shuo Yang, Xin Chen, et al.
Genetic Testing and Molecular Biomarkers|April 29, 2025
Spectrum and Frequencies of Genes for Inherited Hearing Loss in Southwestern Chinese FamiliesYuanyuan Xiao, Li Wang, Cong Zhou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 15, 2025
[Analysis of TYR gene variant in a patient with Oculocutaneous albinism]Xiaolei Jin, Hanbing Xie, Ping Wang, et al.
Oncology Reports|March 12, 2015
Paris saponin II inhibits human ovarian cancer cell-induced angiogenesis by modulating NF-κB signalingMei Yang, Juan Zou, Hongmei Zhu, et al.
Journal of Human Genetics|May 20, 2024
Homozygous variant in DRC3 (LRRC48) gene causes asthenozoospermia and male infertilityJiao Qin, Jinyu Wang, Jianhai Chen, et al.
Molecular Genetics & Genomic Medicine|June 5, 2023
A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney diseaseQianying Zhao, Yu Tan, Xiao Xiao, et al.
Journal of Clinical Laboratory Analysis|August 17, 2021
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencingMei Yang, Hanbing Xie, Bocheng Xu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 29, 2019
[Prenatal diagnosis for a pregnant woman affected with Williams-Beuren syndrome]Na Xi, Zhu Zhang, Xueyan Wang, et al.
International Journal of Oncology|November 21, 2019
Long non‑coding RNAs in HBV‑related hepatocellular carcinoma (Review)Hao Zhang, Xuebing Chen, Jian Zhang, et al.
Frontiers in Genetics|April 3, 2025
Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3Jingqun Mai, Zhu Zhang, Bocheng Xu, et al.
Pageof 18

Showing results (71-80 of 175) with videos related to

Sort By:
Pageof 18
Prenatal Diagnosis|November 4, 2025
Microcephaly, Cerebellar Hypoplasia, Enlarged Posterior Fossa and Polyhydramnios: Prenatal Phenotypes for CASK-Related DisordersJing Chen, Shuo Yang, Xin Chen, et al.
Genetic Testing and Molecular Biomarkers|April 29, 2025
Spectrum and Frequencies of Genes for Inherited Hearing Loss in Southwestern Chinese FamiliesYuanyuan Xiao, Li Wang, Cong Zhou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 15, 2025
[Analysis of TYR gene variant in a patient with Oculocutaneous albinism]Xiaolei Jin, Hanbing Xie, Ping Wang, et al.
Oncology Reports|March 12, 2015
Paris saponin II inhibits human ovarian cancer cell-induced angiogenesis by modulating NF-κB signalingMei Yang, Juan Zou, Hongmei Zhu, et al.
Journal of Human Genetics|May 20, 2024
Homozygous variant in DRC3 (LRRC48) gene causes asthenozoospermia and male infertilityJiao Qin, Jinyu Wang, Jianhai Chen, et al.
Molecular Genetics & Genomic Medicine|June 5, 2023
A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney diseaseQianying Zhao, Yu Tan, Xiao Xiao, et al.
Journal of Clinical Laboratory Analysis|August 17, 2021
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole-exome sequencingMei Yang, Hanbing Xie, Bocheng Xu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 29, 2019
[Prenatal diagnosis for a pregnant woman affected with Williams-Beuren syndrome]Na Xi, Zhu Zhang, Xueyan Wang, et al.
International Journal of Oncology|November 21, 2019
Long non‑coding RNAs in HBV‑related hepatocellular carcinoma (Review)Hao Zhang, Xuebing Chen, Jian Zhang, et al.
Frontiers in Genetics|April 3, 2025
Case report: Inflammatory bowel disease in Hermansky-Pudlak syndrome type 3 due to novel variant in HPS3Jingqun Mai, Zhu Zhang, Bocheng Xu, et al.
Pageof 18