Specific phenotype semantics facilitate gene prioritization in clinical exome sequencing

بواسطة Tomar, S, Sethi, R, Lai, PS
منشور في 2020

Pharmaceutical care issues encountered by post-menopausal osteoporotic women prescribed bisphosphonates

بواسطة Lai, P.S., Chua, S.S., Chan, S.P.
منشور في 2012

Impact of pharmaceutical care on knowledge, quality of life and satisfaction of postmenopausal women with osteoporosis

بواسطة Lai, P.S., Chua, S.S., Chan, S.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

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

J’Accuse…. Or The Plight of pro-bono Volunteer Scientists in Academic Publishing

بواسطة Reichardt, JKV, Patrinos, GP, Lai, PS, Novelli, G
منشور في 2022

Efficient mining of haplotype patterns for linkage disequilibrium mapping

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

Validation of the diabetes, hypertension and hyperlipidemia (DHL) knowledge instrument in Malaysia

بواسطة Lai, P.S., Chua, S.S., Tan, C.H., Chan, S.P.
منشور في 2012

The impact of pharmacist intervention on the use of activated vitamin D in a tertiary referral hospital in Malaysia

بواسطة Siow, J.Y., Lai, P.S., Chua, S.S., Chan, S.P.
منشور في 2009

The validity and reliability of the Malaysian osteoporosis knowledge Tool in postmenopausal women

بواسطة Lai, P.S., Chua, S.S., Chan, S.P., Low, W.Y.
منشور في 2008

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

Development and validation of the osteoporosis patient satisfaction questionnaire (OPSQ)

بواسطة Lai, P.S., Chua, S.S., Chan, S.P., Low, W.Y., Wong, I.C.
منشور في 2010

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

Novel frameshift variant in the PCNT gene associated with Microcephalic Osteodysplastic Primordial Dwarfism (MOPD) Type II and small kidneys

بواسطة Hettiarachchi, D, Subasinghe, SMV, Anandagoda, GG, Panchal, H, Lai, PS, Dissanayake, VHW
منشور في 2022

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