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Siong-Chuan, Samuel Chong

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Full Name
Siong-Chuan, Samuel Chong
Variants
Chong S.S.
Chong, S.
Chong, S.S.
Chong, S.S.C.
 
Main Affiliation
 
Faculty
 
Email
paecs@nus.edu.sg
 

Publications

Results 81-93 of 93 (Search time: 0.005 seconds).

Issue DateTitleAuthor(s)
819-Mar-2022Single-Tube Screen for Rapid Detection of Repeat Expansions in Seven Common Spinocerebellar AtaxiasLian, Mulias; Limwongse, Chanin; Yoon, Chui-Sheun; Lee, Caroline G ; Law, Hai-Yang ; Chong, Samuel S 
22010Spatially addressable bead-based biosensor for rapid detection of beta-thalassemia mutationsNg, J.K.-K.; Chong, S.S. ; Wang, W.; Liu, W.-T. 
32004Spinocerebellar Ataxia Type 2 with Focal Epilepsy - An Unusual AssociationTan, N.C.K.; Lee, W.L.; Zhou, Y. ; Tan, A.S.C.; Chong, S.S. 
42009Successful preimplantation genetic diagnosis of Hb Bart's hydrops fetalis in Singapore after fresh and frozen embryo replacement cyclesYap, C.; Tan, A.S.C.; Chong, S.S. ; Lim, M.N.; Wang, W.; Tan, W.C.
52010Tgfβ3 regulation of chondrogenesis and osteogenesis in zebrafish is mediated through formation and survival of a subpopulation of the cranial neural crestCheah, F.S.H.; Chong, S.S. ; Winkler, C. ; Jabs, E.W.
62007The authors of the article cited above respond [4]Choolani, M. ; Yee, S.H.S.; Chong, S. 
72006The promoter region of the MDR1 gene is largely invariant, but different single nucleotide polymorphism haplotypes affect MDR1 promoter activity differently in different cell linesWang, B.; Ngoi, S.; Lee, C.G.L. ; Wang, J. ; Chong, S.S. 
81-Dec-2019Towards precision medicine: interrogating the human genome to identify drug pathways associated with potentially functional, population-differentiated polymorphismsBachtiar, Maulana ; Ooi, Brandon Nick Sern ; Wang, Jingbo ; Jin, Yu; Tan, Tin Wee ; Chong, Samuel S ; Lee, Caroline GL 
92005Unusual rearrangement of the α-globin gene cluster containing both the -α3.7and αααanti-4.2crossover junctions: Clinical diagnostic implications and possible mechanismsWang, W. ; Chong, S.S. ; Chan, A.Y.Y.; Chan, L.-C.; Ma, E.S.K.
108-Aug-2022Using genome wide studies to generate and test hypotheses that provide mechanistic details of how synonymous codons affect protein structure and function: Functional SNPs in the age of precision medicineOoi, BNS ; Lim, AJW ; Chong, SS ; Lee, CGL 
112017Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 geneLim G.X.Y.; Yeo M.; Koh Y.Y.; Winarni T.I.; Rajan-Babu I.-S.; Chong S.S. ; Faradz S.M.H.; Guan M.
12Apr-2013X-linked markers in the Duchenne muscular dystrophy gene associated with oral cleftsPatel, P.J.; Beaty, T.H.; Ruczinski, I.; Murray, J.C.; Marazita, M.L.; Munger, R.G.; Hetmanski, J.B.; Wu, T.; Murray, T.; Rose, M.; Redett, R.J.; Jin, S.C.; Lie, R.T.; Wu-Chou, Y..-H.; Wang, H. ; Ye, X.; Yeow, V.; Chong, S. ; Jee, S.H.; Shi, B.; Scott, A.F.
132007Zebrafish twist1 is expressed in craniofacial, vertebral, and renal precursorsYeo, G.-H.; Cheah, F.S.H.; Chong, S.S. ; Jabs, E.W.