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Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
October 18, 2017
[Research progress on the safety of offsprings conceived by assisted reproductive technology]
Liya Wang, Yeqing Qian, Fan Jin
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
January 5, 2020
[Genetic analysis of a family of Van der Woude syndrome]
Yuqing Xu, Yeqing Qian, Weimiao Yao, et al.
Frontiers in Pediatrics
|
July 5, 2023
Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of <i>LAMA2</i> gene
Yuqing Xu, Linyan Zhu, Yeqing Qian, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
October 18, 2017
[Single nucleotide polymorphism-array in genetic analysis of chorionic villi from early spontaneous miscarriages]
Yixi Sun, Yuqin Luo, Yeqing Qian, et al.
Frontiers in Genetics
|
October 24, 2022
Case Report: Novel splicing mutations in <i>RFX5</i> causing MHC class II deficiency
Shan Chen, Yuqing Xu, Yeqing Qian, et al.
The Journal of International Medical Research
|
October 3, 2024
Squamous cell carcinoma of the cervix associated with choriocarcinomatous differentiation: a case report and review of the literature
Fenfen Wang, Shanshan Xu, Xiaofei Zhang, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
November 19, 2020
[Genetic analysis and clinical phenotype of a family with lymphedema-distichiasis syndrome]
Gang Hu, Bei Liu, Min Chen, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
November 19, 2020
[Genetic analysis of a mosaic case with low proportion mutation of <i>TSC2</i> gene]
Xiaoxiao Jin, Pengzhen Jin, Kai Yan, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 2021
Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings
Bei Liu, Mengjia Chen, Yanmei Yang, et al.
Frontiers in Genetics
|
July 11, 2022
Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)
Lihong Fan, Pengzhen Jin, Yeqing Qian, et al.
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Search research articles
Search
Showing results (1-10 of 57) with videos related to
Sort By:
Page
of 6
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
October 18, 2017
[Research progress on the safety of offsprings conceived by assisted reproductive technology]
Liya Wang, Yeqing Qian, Fan Jin
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
January 5, 2020
[Genetic analysis of a family of Van der Woude syndrome]
Yuqing Xu, Yeqing Qian, Weimiao Yao, et al.
Frontiers in Pediatrics
|
July 5, 2023
Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of <i>LAMA2</i> gene
Yuqing Xu, Linyan Zhu, Yeqing Qian, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
October 18, 2017
[Single nucleotide polymorphism-array in genetic analysis of chorionic villi from early spontaneous miscarriages]
Yixi Sun, Yuqin Luo, Yeqing Qian, et al.
Frontiers in Genetics
|
October 24, 2022
Case Report: Novel splicing mutations in <i>RFX5</i> causing MHC class II deficiency
Shan Chen, Yuqing Xu, Yeqing Qian, et al.
The Journal of International Medical Research
|
October 3, 2024
Squamous cell carcinoma of the cervix associated with choriocarcinomatous differentiation: a case report and review of the literature
Fenfen Wang, Shanshan Xu, Xiaofei Zhang, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
November 19, 2020
[Genetic analysis and clinical phenotype of a family with lymphedema-distichiasis syndrome]
Gang Hu, Bei Liu, Min Chen, et al.
Zhejiang Da Xue Xue Bao. Yi Xue Ban = Journal of Zhejiang University. Medical Sciences
|
November 19, 2020
[Genetic analysis of a mosaic case with low proportion mutation of <i>TSC2</i> gene]
Xiaoxiao Jin, Pengzhen Jin, Kai Yan, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 15, 2021
Identification of of a PAX2 mutation from maternal mosaicism causes recurrent renal disorder in siblings
Bei Liu, Mengjia Chen, Yanmei Yang, et al.
Frontiers in Genetics
|
July 11, 2022
Case Report: Prenatal Diagnosis of Postaxial Polydactyly With Bi-Allelic Variants in Smoothened (SMO)
Lihong Fan, Pengzhen Jin, Yeqing Qian, et al.
Page
of 6