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Page 1
Prenatal genetic diagnosis of tetrasomy 18p from maternal trisomy 18p: a case report.
Mol Cytogenet. 2022 Jun 27;15(1):25. doi: 10.1186/s13039-022-00602-4.
Mol Cytogenet. 2022.
PMID: 35761312
Free PMC article.
Biochemical and genetic characteristics of 40 neonates with carnitine deficiency.
Zhou X, Teng Y, Lin-Peng S, Li Z, Wu L, Liang D.
Zhou X, et al. Among authors: lin peng s.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020 Oct 28;45(10):1164-1171. doi: 10.11817/j.issn.1672-7347.2020.190241.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020.
PMID: 33268576
Free article.
Chinese, English.
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In situ genetic correction of F8 intron 22 inversion in hemophilia A patient-specific iPSCs.
Wu Y, Hu Z, Li Z, Pang J, Feng M, Hu X, Wang X, Lin-Peng S, Liu B, Chen F, Wu L, Liang D.
Wu Y, et al. Among authors: lin peng s.
Sci Rep. 2016 Jan 8;6:18865. doi: 10.1038/srep18865.
Sci Rep. 2016.
PMID: 26743572
Free PMC article.
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[Establishment of hemophilia A patient-specific inducible pluripotent stem cells with urine cells].
Hu Z, Hu X, Pang J, Wang X, Lin Peng S, Li Z, Wu Y, Wu L, Liang D.
Hu Z, et al. Among authors: lin peng s.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Oct;32(5):609-14. doi: 10.3760/cma.j.issn.1003-9406.2015.05.001.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015.
PMID: 26418976
Chinese.
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The genetics and clinical outcomes in 151 cases of fetal growth restriction: A Chinese single-center study.
Peng C, Hu L, Bu X, Li H, Jiang X, Zhou S, Deng L, He J, LinPeng S.
Peng C, et al.
Eur J Obstet Gynecol Reprod Biol. 2024 May 11;298:128-134. doi: 10.1016/j.ejogrb.2024.05.004. Online ahead of print.
Eur J Obstet Gynecol Reprod Biol. 2024.
PMID: 38756052
Free article.
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[Mutation analysis of EXT genes in two pedigrees with hereditary multiple exostoses].
Deng LB, Quan Y, Liu J, Lin Peng SY, Liang DS, Wu LQ.
Deng LB, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Dec;30(6):641-4. doi: 10.3760/cma.j.issn.1003-9406.2013.06.001.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013.
PMID: 24327137
Chinese.
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