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Frontiers in Genetics|February 4, 2020
Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore PlatformLiang Hu, Fan Liang, Dehua Cheng, et al.Reproductive Biomedicine Online|May 1, 2021
Reproductive risks and preimplantation genetic testing intervention for X-autosome translocation carriersShimin Yuan, Dehua Cheng, Keli Luo, et al.Human Reproduction (Oxford, England)|May 16, 2023
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermiaWeili Wang, Lilan Su, Lanlan Meng, et al.Molecular Cytogenetics|February 15, 2018
Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literatureHaiyu Li, Juan Du, Wen Li, et al.Human Genetics|January 17, 2020
Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCDChaofeng Tu, Hongchuan Nie, Lanlan Meng, et al.Reproductive Biomedicine Online|June 20, 2025
Preimplantation genetic testing for facioscapulohumeral dystrophy caused by contractions of 4q35 D4Z4 repeatsXiao Hu, Weili Wang, Dehua Cheng, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 15, 2022
Segmental aneuploidies with 1 Mb resolution in human preimplantation blastocystsPingyuan Xie, Ping Liu, Shuoping Zhang, et al.Human Reproduction (Oxford, England)|September 6, 2022
A novel multifunctional haplotyping-based preimplantation genetic testing for different genetic conditionsPingyuan Xie, Xiao Hu, Lingyin Kong, et al.Frontiers in Genetics|November 16, 2020
Application of FF-QuantSC for the Precise Estimation of Fetal Fraction in Non-invasive Prenatal Testing in Two SRY-Translocation CasesYan Zeng, Jiong Gao, Hua Yuan, et al.Biology of Reproduction|January 26, 2013
Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocystsXuYang Yin, Ke Tan, Gábor Vajta, et al.Pageof 5