Yu, D., Zhang, K., Han, M., Pan, W., Chen, Y., Wang, Y., . . . Du, Y. (2019). Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing. Mol Genet Genomic Med.
Stile di citazione ChicagoYu, Dongyi, et al. "Noninvasive Prenatal Testing for Fetal Subchromosomal Copy Number Variations and Chromosomal Aneuploidy By Low‐pass Whole‐genome Sequencing." Mol Genet Genomic Med 2019.
Citazione MLAYu, Dongyi, et al. "Noninvasive Prenatal Testing for Fetal Subchromosomal Copy Number Variations and Chromosomal Aneuploidy By Low‐pass Whole‐genome Sequencing." Mol Genet Genomic Med 2019.
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