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A More Universal Approach to Comprehensive Analysis of Thalassemia Alleles (CATSA).
Liang Q, Gu W, Chen P, Li Y, Liu Y, Tian M, Zhou Q, Qi H, Zhang Y, He J, Li Q, Tang L, Tang J, Teng Y, Zhou Y, Huang S, Lu Z, Xu M, Hou W, Huang T, Li Y, Li R, Hu L, Li S, Guo Q, Zhuo Z, Mou Y, Cram DS, Wu L. Liang Q, et al. Among authors: huang t, huang s. J Mol Diagn. 2021 Sep;23(9):1195-1204. doi: 10.1016/j.jmoldx.2021.06.008. Epub 2021 Jul 20. J Mol Diagn. 2021. PMID: 34293487 Free article.
Concurrent newborn hearing and genetic screening of common hearing loss variants with bloodspot-based targeted next generation sequencing in Jiangxi province.
Luo H, Yang Y, Wang X, Xu F, Huang C, Liu D, Zhang L, Huang T, Ma P, Lu Q, Huang S, Yang B, Zou Y, Liu Y. Luo H, et al. Among authors: huang t, huang c, huang s. Front Pediatr. 2022 Oct 31;10:1020519. doi: 10.3389/fped.2022.1020519. eCollection 2022. Front Pediatr. 2022. PMID: 36389375 Free PMC article.
Prenatal chromosomal microarray analysis in a large Chinese cohort of fetuses with congenital heart defects: a single center study.
Lu Q, Luo L, Zeng B, Luo H, Wang X, Qiu L, Yang Y, Feng C, Zhou J, Hu Y, Huang T, Ma P, Huang T, Xie K, Yuan H, Huang S, Yang B, Zou Y, Liu Y. Lu Q, et al. Among authors: huang t, huang s. Orphanet J Rare Dis. 2024 Aug 22;19(1):307. doi: 10.1186/s13023-024-03317-4. Orphanet J Rare Dis. 2024. PMID: 39175064 Free PMC article.
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