A comparison of morbidity patterns in public and private primary care clinics in malaysia
Mimi, O, Tong, Sf, Nordin, S, Teng, Cl, Khoo, Em, Abdul-Rahman, A, Zailinawati, Ah, Lee, Vkm, Chen, Ws, Shihabudin, Wm, Noridah, Ms, Fauziah, Ze
Published in Malaysian family physician (2011)
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Published in Malaysian family physician (2011)
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Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives
Mak, C M, Mok, N S, Shum, H C, Siu, W K, Chong, Y K, Lee, H H C, Fong, N C, Tong, S F, Lee, K W, Ching, C K, Chen, S P L, Cheung, W L, Tso, C B, Poon, W M, Lau, C L, Lo, Y K, Tsui, P T, Shum, S F, Lee, K C
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01.02.2019)
Published in Hong Kong medical journal = Xianggang yi xue za zhi (01.02.2019)
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Journal Article
MECP2 mutation in male patients with non-specific X-linked mental retardation
Orrico, Alfredo, Lam, Ching-Wan, Galli, Lucia, Dotti, Maria Teresa, Hayek, Giuseppe, Tong, Sui-Fan, Poon, Priscilla M.K., Zappella, Michele, Federico, Antonio, Sorrentino, Vincenzo
Published in FEBS letters (22.09.2000)
Published in FEBS letters (22.09.2000)
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Poor blood pressure control and its associated factors among older people with hypertension: A cross-sectional study in six public primary care clinics in Malaysia
Cheong, A T, Sazlina, S G, Tong, S F, Azah, A S, Salmiah, S
Published in Malaysian family physician (2015)
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Published in Malaysian family physician (2015)
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Identification of RASSF1A modulated genes in nasopharyngeal carcinoma
CHOW, L. S.-N, LAM, C.-W, CHAN, S. Y.-Y, TSAO, S.-W, TO, K-F, TONG, S.-F, HUNG, W.-K, DAMMANN, R, HUANG, D. P, LO, K.-W
Published in Oncogene (12.01.2006)
Published in Oncogene (12.01.2006)
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A frequent activated smoothened mutation in sporadic basal cell carcinomas
LAM, C.-W, JINGWU XIE, TO, K.-F, NG, H.-K, LEE, K.-C, YUEN, N. W.-F, LIM, P.-L, CHAN, L. Y.-S, TONG, S.-F, MCCORMICK, F
Published in Oncogene (21.01.1999)
Published in Oncogene (21.01.1999)
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Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria
Yuen, Y.-P., Lam, C.-W., Lai, C.-K., Tong, S-F, Li, P.-S., Tam, S., Kwan, E.Y-W., Chan, S.-Y., Tsang, W.-K., Chan, K.-Y., Mak, W.-L., Cheng, C.-W., Chan, Y.-W.
Published in Kidney international (01.01.2006)
Published in Kidney international (01.01.2006)
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Novel missense mutation (Y279S) in the GLRA1 gene causing hyperekplexia
Poon, Wing-Tat, Chan, Kwok-Yin, Au, Kam-Ming, Tong, Sui-Fan, Chan, Yan-Wo, Lam, Ching-Wan, Chow, Chun-Bong
Published in Clinica chimica acta (01.02.2006)
Published in Clinica chimica acta (01.02.2006)
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Mutation of Proline 409 to Arginine in the Meander Region of Cytochrome P450c17 Causes Severe 17α-Hydroxylase Deficiency
Lam, Ching-Wan, Arlt, Wiebke, Chan, Chi-Kwok, Honour, John W., Lin, Chin Jia, Tong, Sui-Fan, Choy, Kwong-Wai, Miller, Walter L.
Published in Molecular genetics and metabolism (01.03.2001)
Published in Molecular genetics and metabolism (01.03.2001)
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Galactorrhea—A strong clinical clue towards the diagnosis of neurotransmitter disease
Yeung, Wai Lan, Lam, Ching Wan, Hui, Joannie, Tong, Sui Fan, Wu, Shun Ping
Published in Brain & development (Tokyo. 1979) (01.07.2006)
Published in Brain & development (Tokyo. 1979) (01.07.2006)
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Juvenile-onset glycogen storage disease type II with novel mutations in acid alpha-glucosidase gene
Lam, C W, Yuen, Y P, Chan, K Y, Tong, S F, Lai, C K, Chow, T C, Lee, K C, Chan, Y W, Martiniuk, F
Published in Neurology (25.02.2003)
Published in Neurology (25.02.2003)
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