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Molecular genetics of tetrahydrobiopterin deficiency in Chinese patients.
Li N, Yu P, Rao B, Deng Y, Guo Y, Huang Y, Ding L, Zhu J, Yang H, Wang J, Guo J, Chen F, Liu Z. Li N, et al. Among authors: rao b. J Pediatr Endocrinol Metab. 2018 Aug 28;31(8):911-916. doi: 10.1515/jpem-2018-0037. J Pediatr Endocrinol Metab. 2018. PMID: 30001213
A short-read multiplex sequencing method for reliable, cost-effective and high-throughput genotyping in large-scale studies.
Cao H, Wang Y, Zhang W, Chai X, Zhang X, Chen S, Yang F, Zhang C, Guo Y, Liu Y, Tang Z, Chen C, Xue Y, Zhen H, Xu Y, Rao B, Liu T, Zhao M, Zhang W, Li Y, Zhang X, Tellier LC, Krogh A, Kristiansen K, Wang J, Li J. Cao H, et al. Among authors: rao b. Hum Mutat. 2013 Dec;34(12):1715-20. doi: 10.1002/humu.22439. Epub 2013 Oct 7. Hum Mutat. 2013. PMID: 24014314
Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder.
Li SJ, Yu SS, Luo HY, Li X, Rao B, Wang Y, Li ZZ, Liu G, Zou LP, Zhang JS, Feng C, Liu J, Liu JW, Hu N, Chen XQ, Yu SY, Li K, He MW, Yu XG, Wang J, Guo SL, Chen ZY, Zhang L, Ma L. Li SJ, et al. Among authors: rao b. Clin Chim Acta. 2018 Apr;479:144-147. doi: 10.1016/j.cca.2018.01.025. Epub 2018 Feb 2. Clin Chim Acta. 2018. PMID: 29366832
Characterization of 236 novel alleles at the HLA-A, -B, -C, -DRB1, -DQB1 and -DPB1 loci from China Marrow Donor Program.
Li J, Qu J, Zhang X, Zhang C, Liu Y, Cao H, Zhang W, Wang Y, Chen H, Chen G, Zheng Z, Shen M, Cheng Z, Tang J, Zhen H, Liao K, Chen C, Yang H, Tian Z, Zhang H, Hua S, Rao B, Wang N, Zhang Q, Liu T, Chen S, Wang L, Yi X. Li J, et al. Among authors: rao b. Tissue Antigens. 2011 Oct;78(4):267-70. doi: 10.1111/j.1399-0039.2011.01731.x. Epub 2011 Jul 7. Tissue Antigens. 2011. PMID: 21732917
2,610 results