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Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders.
Szot JO, Campagnolo C, Cao Y, Iyer KR, Cuny H, Drysdale T, Flores-Daboub JA, Bi W, Westerfield L, Liu P, Leung TN, Choy KW, Chapman G, Xiao R, Siu VM, Dunwoodie SL. Szot JO, et al. Among authors: leung tn. Am J Hum Genet. 2020 Jan 2;106(1):129-136. doi: 10.1016/j.ajhg.2019.12.006. Epub 2019 Dec 26. Am J Hum Genet. 2020. PMID: 31883644 Free PMC article.
Rapid clearance of fetal DNA from maternal plasma.
Lo YM, Zhang J, Leung TN, Lau TK, Chang AM, Hjelm NM. Lo YM, et al. Among authors: leung tn. Am J Hum Genet. 1999 Jan;64(1):218-24. doi: 10.1086/302205. Am J Hum Genet. 1999. PMID: 9915961 Free PMC article.
Hypermethylation of RASSF1A in human and rhesus placentas.
Chiu RW, Chim SS, Wong IH, Wong CS, Lee WS, To KF, Tong JH, Yuen RK, Shum AS, Chan JK, Chan LY, Yuen JW, Tong YK, Weier JF, Ferlatte C, Leung TN, Lau TK, Lo KW, Lo YM. Chiu RW, et al. Among authors: leung tn. Am J Pathol. 2007 Mar;170(3):941-50. doi: 10.2353/ajpath.2007.060641. Am J Pathol. 2007. PMID: 17322379 Free PMC article.
Genetic screening and diagnosis.
Lau TK, Leung TN. Lau TK, et al. Among authors: leung tn. Curr Opin Obstet Gynecol. 2005 Apr;17(2):163-9. doi: 10.1097/01.gco.0000162187.99219.e0. Curr Opin Obstet Gynecol. 2005. PMID: 15758610 Review.
137 results