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Number of items: 5.


Choong, S.S. and Latiff, Z.A. and Mohamed, M. and Lim, L.L.W. and Chen, K.S. and Vengidasan, L. and Razali, H. and Abdul Rahman, E.J. and Ariffin, H. (2012) Childhood adrenocortical carcinoma as a sentinel cancer for detecting families with germline TP53 mutations. Clinical Genetics. ISSN 0009-9163,


Sow, A.J. and Ramli, R. and Latiff, Z.A. and Ichikawa, S. and Gray, A.K. and Nordin, R. and Abd Jabar, M.N. and Putra, S.H.A.P. and Siar, C.H. and Econs, M.J. (2010) Osteoglophonic dysplasia: A `common' mutation in a rare disease. Clinical Genetics, 78 (2). pp. 197-198. ISSN 0009-9163,


Tsai, Meng Han and Chan, Chung Kin and Chang, Ying Chao and Yu, Y.T. and Chuang, S.T. and Fan, W.L. and Ling, S.C. and Fu, Ting Ying and Chang, Wen Neng and Liou, Chia Wei and Chuang, Yao Chung and Ng, Ching Ching and Hwang, Daw Yang and Lim, Kheng Seang (2017) DEPDC5 mutations in familial and sporadic focal epilepsy. Clinical Genetics, 92 (4). pp. 397-404. ISSN 0009-9163, DOI


Yang, W. and Lee, P.P.W. and Thong, Meow Keong and Ramanujam, T.M. and Shanmugam, A. and Koh, M.T. and Chan, K.W. and Ying, D. and Wang, Y. and Shen, J.J. and Yang, J. and Lau, Y.L. (2015) Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency. Clinical Genetics, 88 (6). pp. 542-549. ISSN 0009-9163, DOI


Zhao, Y. and Gopalai, A.A. and Ahmad-Annuar, A. and Teng, E.W.L. and Prakash, K.M. and Tan, L.C.S. and Au, W.L. and Li, H.H. and Lim, Shen Yang and Lim, Soo Kun and Chong, Yip Boon and Tan, Li Ping and Ibrahim, N.M. and Tan, E.K. (2012) Association of HLA locus variant in Parkinson's disease. Clinical Genetics, 84 (5). pp. 501-504. ISSN 0009-9163, DOI

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