A two-stage approach identifies a Q344X mutation in the rhodopsin gene of a Chinese Singaporean family with autosomal dominant retinitis pigmentosa

بواسطة Yong, R.Y.Y., Chee, C.K.L., Yap, E.P.H.
منشور في 2016

A molecular approach for identifying individuals with Li-Fraumeni syndrome who have a limited family history

بواسطة Ang, P., Lim, I.H.K., Yong, R.Y.Y., Lee, A.S.G.
منشور في 2015

Association between an intronic apolipoprotein E polymorphism and bone mineral density in Singaporean Chinese females

بواسطة Tong, T.Y.Y., Mok, H.P.P., Yong, E.L., Yong, R.Y.Y., Chong, A.P.L., Yap, E.P.H., Moochhala, S., Goh, V.H.H., Liang, S.
منشور في 2011

Identification of an I Na-dependent and I to-mediated proarrhythmic mechanism in cardiomyocytes derived from pluripotent stem cells of a Brugada syndrome patient

بواسطة Ma D., Liu Z., Loh L.J., Zhao Y., Li G., Liew R., Islam O., Wu J., Chung Y.Y., Teo W.S., Ching C.K., Tan B.Y., Chong D., Ho K.L., Lim P., Yong R.Y.Y., Panama B.K., Kaplan A.D., Bett G.C.L., Ware J., Bezzina C.R., Verkerk A.O., Cook S.A., Rasmusson R.L., Wei H.
منشور في 2018

Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia

بواسطة Khor, C.C., Miyake, M., Chen, L.J., Shi, Y., Barathi, V.A., Qiao, F., Nakata, I., Yamashiro, K., Zhou, X., Tam, P.O.S., Cheng, C.-Y., Tai, E.S., Vithana, E.N., Aung, T., Teo, Y.-Y., Wong, T.-Y., Moriyama, M., Ohno-Matsui, K., Mochizuki, M., Matsuda, F., Yong, R.Y.Y., Yap, E.P.H., Yang, Z., Pang, C.P., Saw, S.-M., Yoshimura, N.
منشور في 2014