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Issue DateTitleAuthor(s)
2016Alternative splicing of a cryptic exon embedded in intron 6 of SMN1 and SMN2Yoshimoto, S; Harahap, N.I.F; Hamamura, Y; Ar Rochmah, M; Shima, A; Morisada, N; Shinohara, M; Saito, T; Saito, K; Lai, P.S ; Matsuo, M; Awano, H; Morioka, I; Iijima, K; Nishio, H
2009Automated DNA mutation detection using universal conditions direct sequencing: Application to ten muscular dystrophy genesBennett, R.R.; Schneider, H.E.; Estrella, E.; Burgess, S.; Barrett, C.; Beggs, A.H.; Kunkel, L.M.; Cheng, A.S.; Lip, V.; Shen, Y.; Wu, B.-L.; Lai, P.S. ; Darras, B.T.
Feb-2008Characterization of a novel S13F desmin mutation associated with desmin myopathy and heart block in a Chinese familyPica, E.C.; Kathirvel, P.; Pramono, Z.A.D.; Lai, P.-S. ; Yee, W.-C.
2002Comparative study on deletions of the dystrophin gene in three asian populationsLai, P.-S. ; Takeshima, Y.; Adachi, K.; Van Tran, K.; Nguyen, H.T.; Low, P.-S. ; Matsuo, M.
1991Consanguinity and health [19]Tay, J.S.H. ; Lai, P.-S. 
2009Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicingChen, H.Y.; Kathirvel, P.; Yee, W.C.; Lai, P.S. 
28-Aug-2018Data from: Association between the dopamine D4 receptor gene exon III variable number of tandem repeats and political attitudes in female Han ChineseEbstein, Richard P. ; Monakhov, Mikhail V. ; Lu, Yunfeng ; Jiang, Yushi; Lai, Poh San ; Chew, Soo Hong 
1992Deletion analysis of DMD/BMD children in Singapore using multiplex polymerase chain reaction (PCR) techniqueLai, P.S. ; Tay, J.S.H. ; Low, P.S. ; Lee, W.L. ; Koh, G.A.S.; Gan, G.C.
1992Deletional types of alpha-thalassaemia in central JavaTan, J.A.M.A. ; Tay, J.S.H. ; Soemantri, A.; Kham, S.K.Y.; Wong, H.B. ; Lai, P.S. ; Saha, N. 
1997Detection of Low Numbers of Neuroblastoma Cells in VitroLai, P.S. ; Chee, S.; Chiu, L.L. ; Sano, K.
2006Diagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell linesTay, S.K.H.; Khng, H.H.; Low, P.S. ; Lai, P.S. 
2010Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophyQin, W.J.; Yung, L.-Y.L. ; Yim, O.S. ; Lai, P.S. 
2008Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotidesPramono, Z.A.D.; Wang, J.L.; Yee, W.C.; Wee, K.B.; MacDorman, K.F.; Lai, P.S. 
1990Dystrophin function: Calcium-related rather than mechanicalTay, J.S.H. ; Low, P.S. ; Lee, W.L. ; Lai, P.S. ; Gan, G.C.
2007ECTracker-an efficient algorithm for haplotype analysis and classificationLin, L. ; Wong, L. ; Leong, T.-Y. ; Lai, P. 
2003Ethnic variations of a retinoblastoma susceptibility gene (RB1) polymorphism in eight Asian populationsKadam-Pai, P.; Su, X.-Y.; Heng, C.-K. ; Lai, P.-S. ; Miranda, J.J.; Soemantri, A.; Saha, N.
2018Genetic Variation in the Maternal Oxytocin System Affects Cortisol Responsiveness to Breastfeeding in Infants and MothersKrol K.M.; Monakhov M. ; Lai P.S. ; Ebstein R.P. ; Heinrichs M.; Grossmann T.
2009High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastomaPriya, K.; Jada, S.R. ; Poh, S.L. ; Boon, L.Q.; Thuan, C.Q. 
2009High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastomaPriya, K. ; Jada, S.R. ; Poh, S.L. ; Boon, L.Q.; Thuan, C.Q.
2009Identification and characterisation of human dysferlin transcript variants: Implications for dysferlin mutational screening and isoformsPramono, Z.A.D.; Yee, W.C.; Tan, C.L.; Seah, I.A.L.; See, J.S.L.; Kam, S.Y.; Lai, P.S.