Lin Li, MD, PhD

Title(s)Postdoctoral Scholar, Ob/Gyn, Reproductive Sciences
SchoolSchool of Medicine
Address550 16th Street
San Francisco CA 94158
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    1. Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies. Ultrasound Obstet Gynecol. 2020 04; 55(4):502-509. Li L, He Z, Huang X, Lin S, Wu J, Huang L, Wan Y, Fang Q. PMID: 30977228.
      View in: PubMed   Mentions:    Fields:    
    2. miRNA-210-3p regulates trophoblast proliferation and invasiveness through fibroblast growth factor 1 in selective intrauterine growth restriction. J Cell Mol Med. 2019 06; 23(6):4422-4433. Li L, Huang X, He Z, Xiong Y, Fang Q. PMID: 30993882.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    3. Prenatal diagnosis of Pallister-Killian syndrome in one twin. Clin Case Rep. 2018 Aug; 6(8):1470-1473. Li L, Huang L, Huang X, Lin S, He Z, Fang Q. PMID: 30147884.
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    4. Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twins. Prenat Diagn. 2018 04; 38(5):318-327. Zhang Y, Huang L, Huang X, He Z, Lin S, Wang Y, Li L, Luo Y, Fang Q. PMID: 29460287.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. Fetal Aneuploidy: A Comparison of Dichorionic Twins and Monochorionic Twins. Fetal Diagn Ther. 2018; 44(2):124-128. Shi X, Li L, Huang X, Chen B, Zhou Y, Fang Q. PMID: 28869935.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    6. Successful management of a hydropic fetus with severe anemia and thrombocytopenia caused by anti-CD36 antibody. Int J Hematol. 2018 Feb; 107(2):251-256. Xu X, Li L, Xia W, Ding H, Chen D, Liu J, Deng J, Chen Y, He Z, Wang J, Shao Y, Santoso S, Ye X, Fang Q. PMID: 28815406.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    7. Prenatal treatment of severe fetal hemolytic disease due to anti-M alloimmunization by serial intrauterine transfusions. Taiwan J Obstet Gynecol. 2017 Jun; 56(3):379-381. Li L, Huang L, Luo G, Luo Y, Fang Q. PMID: 28600054.
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    8. Discordant phenotypes in monozygotic twins with 16p11.2 microdeletions including the SH2B1 gene. . 2017 Aug; 173(8):2284-2288. Li L, Huang L, Lin S, Luo Y, Fang Q. PMID: 28544142.
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    9. Differing Microdeletion Sizes and Breakpoints in Chromosome 7q11.23 in Williams-Beuren Syndrome Detected by Chromosomal Microarray Analysis. Mol Syndromol. 2016 Feb; 6(6):268-75. Li L, Huang L, Luo Y, Huang X, Lin S, Fang Q. PMID: 27022327.
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