The antecedents of salespeople's relational behaviors

by Guo, L., Ng, I.C.L.
Published 2016

The strategic role of unused service capacity

by Ng, I.C.L., Wirtz, J., Lee, K.S.
Published 2013

An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature

by Ng, I.S.L., Chin, W.-H., Lim, E.C.P., Tan, E.-C.
Published 2014

FMR1 CGG repeat patterns and flanking haplotypes in three Asian populations and their relationship with repeat instability

by Zhou, Y., Chong, S.S., Tang, K., Lee, C.G.L., Law, H.-Y., Ng, I.S.L.
Published 2011

Role of cadherin-17 in oncogenesis and potential therapeutic implications in hepatocellular carcinoma

by Lee, N.P., Poon, R.T.P., Shek, F.H., Ng, I.O.L., Luk, J.M.
Published 2016

De novo trisomy 12p in twin girls with different levels of mosaicism

by Lim, E.C.P., Ng, I.S.L., Yong, M.-H., Yon, H.-Y., Brett, M.S.Y., Tan, E.-C.
Published 2014

Lichenification and enlargement of hands and feet: A sign of progressive familial intrahepatic cholestasis with normal γ-glutamyl-transpeptidase

by Ooi, B.C., Phua, K.B., Lee, B.L., Tan, C.E.L., Ng, I.S.L., Quak, S.H.
Published 2016

De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability

by Brett, M.S., Ng, I.S.L., Lim, E.C.P., Yong, M.H., Li, Z., Lai, A., Tan, E.-C.
Published 2014

Proteomics of hepatocellular carcinoma: Serum vimentin as a surrogate marker for small tumors (≤2 cm)

by Sun, S., Poon, R.T.P., Lee, N.P., Yeung, C., Chan, K.L., Ng, I.O.L., Day, P.J.R., Luk, J.M.
Published 2016

Rapid carrier screening for β-thalassemia by single-step allele-specific PCR and detection

by Quek, D.L., Ng, Y.-Y., Tang-Lim, G.-I., Wang, W., Chong, S.S., Tan, A.S.C., Ng, I.S.L., Law, H.-Y.
Published 2011

Determining the cause of patchwork HBA1 and HBA2 genes: Recurrent gene conversion or crossing over fixation events

by Law, H.-Y., Ng, I.S.L., Luo, H.-Y., Steinberg, M.H., Chui, D.H.K., Wang, W., Ho, J.F.V., Chong, S.S., Najmabadi, H.
Published 2011

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis

by Ding C., Chiu R.W.K., Lau T.K., Leung T.N., Chan L.C., Chan A.Y.Y., Charoenkwan P., Ng I.S.L., Law H.-Y., Ma E.S.K., Xu X., Wanapirak C., Sanguansermsri T., Liao C., Tan Jin Ai M.A., Chui D.H.K., Cantor C.R., Lo Y.M.D.
Published 2014

Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

by Beaty, T.H., Hetmanski, J.B., Fallin, M.D., Park, J.W., Sull, J.W., Liang, K.Y., McIntosh, I., Boyadjiev, S.A., Jabs, E.W., Ingersoll, R., Scott, A.F., VanderKolk, C.A., Redett, R.J., Chong, S.S., Cheah, F.S.H., Wu-Chou, Y.H., Chen, P.K., Chiu, Y.F., Yeow, V., Ng, I.S.L., Cheng, J., Huang, S., Ye, X., Wang, H.
Published 2011