Browsing by Author LAI POH SAN

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Showing results 37 to 42 of 42 < previous 
Issue DateTitleAuthor(s)
1-Nov-2019Resolving the Diagnostic Odyssey of a Patient with an Undefined Neuromuscular Disorder Using Massively Parallel Sequencing ApproachesYu, Yiliu; Ong, Hui Juan; SWATI TOMAR ; TAN LI XUAN, GRACE (CHEN LIXUAN) ; RAMAN SETHI ; TAY KIAT HONG,STACEY ; LAI POH SAN 
2008Screening of dystrophin gene deletions in Malaysian patients with Duchenne Muscular DystrophyMarini, M.; Watihayati, M.S.; Mardziah, M.D.S.; Zahri, M.K.; Hoh, B.P.; Ankathil, R.; Zilfalil, B.A.; Salmi, A.A.; Lai, P.S. 
2003Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: Implications for linkage-disequilibrium gene mappingWeale, M.E.; Depondt, C.; Wood, N.W.; Macdonald, S.J.; Smith, A.; Goldstein, D.B.; Lai, P.S. ; Shorvon, S.D.
1-Sep-2019Specific phenotype semantics facilitate gene prioritization in clinical exome sequencingTomar, S ; Sethi, R; Lai, PS 
22-Oct-2020The orphan nuclear receptor NR0B2 could be a novel susceptibility locus associated with microsatellite-stable, APC mutation-negative early-onset colorectal carcinomas with metabolic manifestation.Lam, Kuen Kuen; RAMAN SETHI ; TAN PING PING, GRACE ; SWATI TOMAR ; Lo, Michelle; Loi, Carol; TANG CHOONG LEONG ; Tan, Emile; LAI POH SAN ; CHEAH PEH YEAN 
1995Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.Lai, P.S. ; Chiu, L.L. ; Low, P.S. ; Lee, W.L. ; Tay, J.S.