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Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment.
Chen HL, Lin PH, Chiang YT, Huang WJ, Lin CF, Ma GC, Chang SP, Fan JY, Lin SY, Wu CC, Chen M. Chen HL, et al. Among authors: lin sy, lin ph, lin cf. Diagnostics (Basel). 2021 Dec 20;11(12):2395. doi: 10.3390/diagnostics11122395. Diagnostics (Basel). 2021. PMID: 34943631 Free PMC article.
Application of molecular cytogenetic techniques to characterize the aberrant Y chromosome arising de novo in a male fetus with mosaic 45,X and solve the discrepancy between karyotyping, chromosome microarray, and multiplex ligation dependent probe amplification.
Lin SY, Lee CN, Peng AY, Yuan TJ, Lee DJ, Lin WH, Ma GC, Chen M. Lin SY, et al. Among authors: lin wh. J Formos Med Assoc. 2018 Nov;117(11):1027-1031. doi: 10.1016/j.jfma.2018.04.011. Epub 2018 May 9. J Formos Med Assoc. 2018. PMID: 29752043 Free article.
Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1.
Chen YL, Hung CC, Lin SY, Fang MY, Tsai YY, Chang LJ, Lee CN, Su YN, Chen SU, Yang YS. Chen YL, et al. Among authors: lin sy. Taiwan J Obstet Gynecol. 2011 Mar;50(1):74-8. doi: 10.1016/j.tjog.2011.01.040. Taiwan J Obstet Gynecol. 2011. PMID: 21482379 Free article.
2,849 results