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Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell Syndrome.
J Pers Med. 2021 Nov 13;11(11):1197. doi: 10.3390/jpm11111197.
J Pers Med. 2021.
PMID: 34834549
Free PMC article.
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Beckwith-Wiedemann Syndrome.
Lin HY, Lee CL, Fran S, Tu RY, Chang YH, Niu DM, Chang CY, Chiu PC, Chou YY, Hsiao HP, Yang CF, Tsai MC, Chu TH, Chuang CK, Lin SP.
Lin HY, et al. Among authors: fran s.
J Pers Med. 2021 Oct 22;11(11):1066. doi: 10.3390/jpm11111066.
J Pers Med. 2021.
PMID: 34834418
Free PMC article.
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Identification and Functional Characterization of IDS Gene Mutations Underlying Taiwanese Hunter Syndrome (Mucopolysaccharidosis Type II).
Lin HY, Tu RY, Chern SR, Lo YT, Fran S, Wei FJ, Huang SF, Tsai SY, Chang YH, Lee CL, Lin SP, Chuang CK.
Lin HY, et al. Among authors: fran s.
Int J Mol Sci. 2019 Dec 23;21(1):114. doi: 10.3390/ijms21010114.
Int J Mol Sci. 2019.
PMID: 31877959
Free PMC article.
Clinical Trial.
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Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15).
Chen CP, Lin HY, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Fran S, Chen YY, Town DD, Pan CW, Wang W.
Chen CP, et al. Among authors: fran s.
Taiwan J Obstet Gynecol. 2020 Jul;59(4):580-585. doi: 10.1016/j.tjog.2020.05.019.
Taiwan J Obstet Gynecol. 2020.
PMID: 32653133
Free article.
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