Consanguinity and health [19]

بواسطة Tay, J.S.H., Lai, P.-S.
منشور في 2014

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

بواسطة Chen Y., Lai P., Piboonrungroj P.
منشور في 2017

LinkageTracker: A discriminative pattern tracking approach to linkage disequilibrium mapping

بواسطة Lin, L., Wong, L., Leong, T., Lai, P.
منشور في 2013

Detection of Low Numbers of Neuroblastoma Cells in Vitro

بواسطة Lai, P.S., Chee, S., Chiu, L.L., Sano, K.
منشور في 2013

ECTracker-an efficient algorithm for haplotype analysis and classification

بواسطة Lin, L., Wong, L., Leong, T.-Y., Lai, P.
منشور في 2014

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

بواسطة Seow, N., Lai, P.S., Yung, L.-Y.L.
منشور في 2014

Efficient mining of haplotype patterns for linkage disequilibrium mapping

بواسطة Lin, L., Wong, L., Leong, T.-Y., Lai, P.S.
منشور في 2013

Efficient mining of haplotype patterns for linkage disequilibrium mapping

بواسطة Lin L., Wong L., Tze-Yun LEONG, Lai P.
منشور في 2010

Mining of Correlated Rules in Genome Sequences

بواسطة Lin, L., Wong, L., Tze-Yun LEONG, Lai, P. S.
منشور في 2002

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

بواسطة Lin, L., Wong, L., Leong, T.Y., Lai, P.
منشور في 2013

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

بواسطة Chen, H.Y., Kathirvel, P., Yee, W.C., Lai, P.S.
منشور في 2011

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

بواسطة Hettiarachchi, D., Panchal, H., Lai, P.S., Dissanayake, V.H.W.
منشور في 2021

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

بواسطة Tay, S.K.H., Khng, H.H., Low, P.S., Lai, P.S.
منشور في 2011

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

بواسطة Qin, W.J., Yung, L.-Y.L., Yim, O.S., Lai, P.S.
منشور في 2011

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

بواسطة Lai, P.S., Chiu, L.L., Low, P.S., Lee, W.L., Tay, J.S.
منشور في 2013

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

بواسطة Loke, K.-Y., Poh, L.K.-S., Lai, P.-S., Lee, W.W.-R.
منشور في 2011

The contributions of oxytocin and vasopressin pathway genes to human behavior

بواسطة Ebstein, R.P., Knafo, A., Mankuta, D., Chew, S.H., Lai, P.S.
منشور في 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)

بواسطة Keng, S.-L., Yim, O.S., Lai, P.S., Chew, S.H., Ebstein, R.P.
منشور في 2021

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

بواسطة Tomar S., Sethi R., Sundar G., Quah T.C., Quah B.L., Lai P.S.
منشور في 2019

Pathogenesis of Duchenne muscular dystrophy: The calcium hypothesis revisited

بواسطة Tay, J.S.H., Lai, P.S., Low, P.S., Lee, W.L., Gan, G.C.
منشور في 2013