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Journal of Ovarian Research|October 19, 2023
Novel immune-related gene signature for risk stratification and prognosis prediction in ovarian cancerHongjun Fei, Xu Han, Yanlin Wang, et al.
Orphanet Journal of Rare Diseases|February 3, 2025
Identification and functional analysis of a novel SMARCC2 splicing variant in a family with syndromic neurodevelopmental disorderMing Li, Jingqi Lin, Hongjun Fei, et al.
Frontiers in Molecular Biosciences|May 31, 2021
Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number VariationsSongchang Chen, Lanlan Zhang, Jiong Gao, et al.
Frontiers in Genetics|December 17, 2020
Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1Songchang Chen, Weihui Shi, Yeqing Qian, et al.
Genome Medicine|December 5, 2025
Universal noninvasive prenatal diagnosis for monogenic disorders using cell-free plasma DNALanlan Zhang, Renyi Hua, Yiming Wu, et al.
Human Reproduction (Oxford, England)|December 11, 2020
Comprehensive preimplantation genetic testing by massively parallel sequencingSongchang Chen, Xuyang Yin, Sijia Zhang, et al.
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