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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|May 31, 2020
[Problems with clinical application of non-invasive prenatal testing]Jianjiang Zhu, Wei Li, Hui Huang, et al.Journal of Microbiology and Biotechnology|October 29, 2025
Microbiome Profiling of Pretreated Human Breast Milk Using Shotgun Metagenomic SequencingQiao Zhang, Yi Zhang, Jianjiang Zhu, et al.Human Genomics|February 24, 2021
cfDNA deconvolution via NIPT of a pregnant woman after bone marrow transplant and donor egg IVFJianjiang Zhu, Feng Hui, Xuequn Mao, et al.Molecular Cytogenetics|December 5, 2021
De novo balanced reciprocal translocation mosaic t(1;3)(q42;q25) detected by prenatal genetic diagnosis: a fetus conceived using preimplantation genetic testing due to a t(12;14)(q22;q13) balanced paternal reciprocal translocationShaoqin Zhang, Jianjiang Zhu, Hong Qi, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 1, 2024
[Comparison of two superparamagnetic purification magnetic beads-based screening and enrichment techniques for isolating cell-free fetal DNA from maternal plasma for non-invasive prenatal screening]Wen Zeng, Jianjiang Zhu, Hong Qi, et al.Frontiers in Genetics|March 10, 2025
Exploration of cfDNA landscape in NIPT and clinical utilities of cfDNA based gene expression inference in prenatal diagnosticsRuo Jia, Jianjiang Zhu, Feng Zhang, et al.Annals of Translational Medicine|July 16, 2021
Whole-exome sequencing analysis to identify novel potential pathogenetic mutations in fetuses with abnormal brain structureLili Shi, Ming Li, Hong Qi, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|July 14, 2015
[Detection of small supernumerary marker chromosome by single nucleotide polymorphism microarray chips]Xiaohui Wen, Hong Qi, Jie Ren, et al.Medicine|April 5, 2019
Prenatal diagnosis of de novo monosomy 18p deletion syndrome by chromosome microarray analysis: Three case reportsHong Qi, Jianjiang Zhu, Shaoqin Zhang, et al.Journal of Clinical Laboratory Analysis|October 17, 2019
Whole-exome sequencing identified compound heterozygous variants in ROR2 gene in a fetus with Robinow syndromeKai Yang, Jianjiang Zhu, Ya Tan, et al.Pageof 2