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Autor:
Lei Gao, Wei Sun, Ze Wu, Wei Song, Xue Jia, Yiyi Xing, Xiaoju Ran, Dan Shan, Jian Zhang, Tianyi Dai
Publikováno v:
OMICS: A Journal of Integrative Biology. 25:738-744
Trisomy 21 is a common birth defect in humans. Screening for trisomy 21 is one of the most important tasks in routine prenatal care and robust noninvasive diagnostics are needed in clinical practice. Urinary proteomics offers a new research platform