Consanguinity and health [19]

由 Tay, J.S.H., Lai, P.-S.
出版 2014

The relationship between airport performance and privatisation policy: A nonparametric metafrontier approach

由 Chen Y., Lai P., Piboonrungroj P.
出版 2017

LinkageTracker: A discriminative pattern tracking approach to linkage disequilibrium mapping

由 Lin, L., Wong, L., Leong, T., Lai, P.
出版 2013

Detection of Low Numbers of Neuroblastoma Cells in Vitro

由 Lai, P.S., Chee, S., Chiu, L.L., Sano, K.
出版 2013

ECTracker-an efficient algorithm for haplotype analysis and classification

由 Lin, L., Wong, L., Leong, T.-Y., Lai, P.
出版 2014

Gold nanostructures for the multiplex detection of glucose-6-phosphate dehydrogenase gene mutations

由 Seow, N., Lai, P.S., Yung, L.-Y.L.
出版 2014

Efficient mining of haplotype patterns for linkage disequilibrium mapping

由 Lin, L., Wong, L., Leong, T.-Y., Lai, P.S.
出版 2013

Efficient mining of haplotype patterns for linkage disequilibrium mapping

由 Lin L., Wong L., Tze-Yun LEONG, Lai P.
出版 2010

Mining of Correlated Rules in Genome Sequences

由 Lin, L., Wong, L., Tze-Yun LEONG, Lai, P. S.
出版 2002

ECTracker--an efficient algorithm for haplotype analysis and classification.

由 Lin, L., Wong, L., Leong, T.Y., Lai, P.
出版 2013

Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing

由 Chen, H.Y., Kathirvel, P., Yee, W.C., Lai, P.S.
出版 2011

Novel variant in NSDHL gene associated with CHILD syndrome and syndactyly- a case report

由 Hettiarachchi, D., Panchal, H., Lai, P.S., Dissanayake, V.H.W.
出版 2021

Diagnostic strategy for the detection of dystrophin gene mutations in Asian patients and carriers using immortalized cell lines

由 Tay, S.K.H., Khng, H.H., Low, P.S., Lai, P.S.
出版 2011

Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy

由 Qin, W.J., Yung, L.-Y.L., Yim, O.S., Lai, P.S.
出版 2011

Usefulness of dinucleotide polymorphism markers in genetic analysis of Duchenne's muscular dystrophy cases in Singapore.

由 Lai, P.S., Chiu, L.L., Low, P.S., Lee, W.L., Tay, J.S.
出版 2013

A case of X-linked adrenal hypoplasia congenita, central precocious puberty and absence of the DAX-1 gene: Implications for pubertal regulation

由 Loke, K.-Y., Poh, L.K.-S., Lai, P.-S., Lee, W.W.-R.
出版 2011

The contributions of oxytocin and vasopressin pathway genes to human behavior

由 Ebstein, R.P., Knafo, A., Mankuta, D., Chew, S.H., Lai, P.S.
出版 2014

Erratum: Association among dispositional mindfulness, self-compassion, and leukocyte telomere length in Chinese adults (BMC Psychol (2019) 7:47 DOI: 10.1186/s40359-019-0323-y)

由 Keng, S.-L., Yim, O.S., Lai, P.S., Chew, S.H., Ebstein, R.P.
出版 2021

Mutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counselling

由 Tomar S., Sethi R., Sundar G., Quah T.C., Quah B.L., Lai P.S.
出版 2019

Pathogenesis of Duchenne muscular dystrophy: The calcium hypothesis revisited

由 Tay, J.S.H., Lai, P.S., Low, P.S., Lee, W.L., Gan, G.C.
出版 2013