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Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10).
Chen CP, Chen M, Ma GC, Chang SP, Chern SR, Chen SW, Wu FT, Lee MS, Wang W. Chen CP, et al. Among authors: chang sp. Taiwan J Obstet Gynecol. 2022 Jan;61(1):132-134. doi: 10.1016/j.tjog.2021.11.021. Taiwan J Obstet Gynecol. 2022. PMID: 35181023 Free article.
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: chang sp. Diagnostics (Basel). 2021 Dec 20;11(12):2395. doi: 10.3390/diagnostics11122395. Diagnostics (Basel). 2021. PMID: 34943631 Free PMC article.
271 results