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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 2, 2023
[The value of combined CNV-Seq and chromosomal karyotyping for the detection of amniocytic mosaicisms and a literature review]Panlai Shi, Ruonan Zhu, Junhong Zhao, et al.
BMC Medical Genomics|March 24, 2021
Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one familyPanlai Shi, Conghui Wang, Yuting Zheng, et al.
Molecular Genetics & Genomic Medicine|September 3, 2019
Influence of validating the parental origin on the clinical interpretation of fetal copy number variations in 141 core family casesPanlai Shi, Rui Li, Conghui Wang, et al.
The Journal of Obstetrics and Gynaecology Research|January 21, 2021
Usefulness of copy number variant detection following monogenic disease exclusion in prenatal diagnosisPanlai Shi, Yanjie Xia, Qianqian Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2021
[Variant analysis of SEC23B gene in 4 families with congenital dyserythropoietic anemia]Yin Feng, Panlai Shi, Ning Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 5, 2022
[Analysis of a case with Mowat-Wilson syndrome due to nonsense variant of ZEB2 gene]Mingcong She, Zhenhua Zhao, Panlai Shi, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 1, 2022
[Prenatal diagnosis of partial deletion of NRXN1 gene with combined CNV-seq and qPCR assays]Lixia Wang, Panlai Shi, Hua'nan Ren, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|November 11, 2024
[Methylation epigenetic analysis of a pedigree affected with Fragile X syndrome based on Nanopore long-read sequencing]Conghui Wang, Panlai Shi, Li'na Liu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2021
[Genetic analysis of a case with Pierre-Robin sequence due to partial 1q trisomy and partial 4q monosomy]Qiuyan Zhang, Shanshan Gao, Li Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 4, 2024
[Clinical and genetic analysis of ten Chinese pedigrees affected with 7q11.23 duplication syndrome]Panlai Shi, Yongchao Liu, Yaqin Hou, et al.
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