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

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

Gonadoblastoma-associated mixed germ cell tumour in 46,XY complete gonadal dysgenesis (Swyer syndrome): Analysis of Y chromosomal genotype and OCT3/4 and TSPY expression profile

بواسطة Ng, S.B., Yong, M.H., Knight, L.A., Lee, V.K.M., Nadarajah, S., Stoop, H., Looijenga, L.H.J.
منشور في 2012

Neurology of COVID-19 in Singapore

بواسطة Koh, JS, De Silva, DA, Quek, AML, Chiew, HJ, Tu, TM, Seet, CYH, Hoe, RHM, Saini, M, Hui, ACF, Angon, J, Ker, JR, Yong, MH, Goh, Y, Yu, WY, Lim, TCC, Tan, BYQ, Ng, KWP, Yeo, LLL, Pang, YZ, Prakash, KM, Ahmad, A, Thomas, T, Lye, DCB, Tan, K, Umapathi, T
منشور في 2020

Neuroblastoma patient-derived cultures are enriched for a mesenchymal gene signature and reflect individual drug response

بواسطة Hee, E., Wong, M.K., Tan, S.H., Choo, Z., Kuick, C.H., Ling, S., Yong, M.H., Jain, S., Lian, D.W.Q., Ng, E.H.Q., Yong, Y.F.L., Ren, M.H., Syed Sulaiman, N., Low, S.Y.Y., Chua, Y.W., Syed, M.F., Lim, T.K.H., Soh, S.Y., Iyer, P., Seng, M.S.F., Lam, J.C.M., Tan, E.E.K., Chan, M.Y., Tan, A.M., Chen, Y., Chen, Z., Chang, K.T.E., Loh, A.H.P.
منشور في 2021