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RAMACHANDRAM, S., KENG, W. T., ARIFFIN, R., GANESAN, V.
Published in Journal of genetics (01.08.2013)
Published in Journal of genetics (01.08.2013)
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Expanding the phenome and variome of skeletal dysplasia
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Published in Genetics in medicine (01.12.2018)
Published in Genetics in medicine (01.12.2018)
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Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency
Brun, L, Ngu, L H, Keng, W T, Ch'ng, G S, Choy, Y S, Hwu, W L, Lee, W T, Willemsen, M A A P, Verbeek, M M, Wassenberg, T, Régal, L, Orcesi, S, Tonduti, D, Accorsi, P, Testard, H, Abdenur, J E, Tay, S, Allen, G F, Heales, S, Kern, I, Kato, M, Burlina, A, Manegold, C, Hoffmann, G F, Blau, N
Published in Neurology (06.07.2010)
Published in Neurology (06.07.2010)
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Clinical, biochemical, and molecular overview of transaldolase deficiency and evaluation of the endocrine function: update of 34 patients
Williams, M, Valayannopoulos, V, Altassan, R, Chung, W K, Heijboer, A C, Keng, W T, Lapatto, R, McClean, P, Mulder, M F, Tylki-Szymańska, A, Walenkamp, M J E, Alfadhel, M, Alakeel, H, Salomons, G S, Eyaid, W, Wamelink, M M C
Published in Journal of inherited metabolic disease (02.05.2018)
Published in Journal of inherited metabolic disease (02.05.2018)
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Willingness to Pay for Cancer Genetic Testing in a Tertiary Healthcare Centre
AN, Aizuddin, SAS, Syed Rusli, AR, Ramdzan, SA, Syed Omar, Z, Mahmud, Z, Abdul Latiff, SA, Shah, S, Amat, F, Ismail, WT, Keng, GS, Ch’ng, H, Rais, SM, Aljunid
Published in International medical journal Malaysia (01.07.2021)
Published in International medical journal Malaysia (01.07.2021)
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A balanced reciprocal translocation in a case of hypomelanosis of Ito with confirmation of mosaicism using buccal cell interphase FISH
Keng, W.T., Harewood, L., Grace, E., Paxton, C., Lam, W.W.K., FitzPatrick, D.R.
Published in American journal of medical genetics. Part A (15.05.2006)
Published in American journal of medical genetics. Part A (15.05.2006)
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Evaluation of Clinical Manifestations in Patients with Severe Lymphedema with and without CCBE1 Mutations
Alders, M., Mendola, A., Adès, L., Al Gazali, L., Bellini, C., Dallapiccola, B., Edery, P., Frank, U., Hornshuh, F., Huisman, S.A., Jagadeesh, S., Kayserili, H., Keng, W.T., Lev, D., Prada, C.E., Sampson, J.R., Schmidtke, J., Shashi, V., van Bever, Y., Van der Aa, N., Verhagen, J.M., Verheij, J.B., Vikkula, M., Hennekam, R.C.
Published in Molecular syndromology (01.03.2013)
Published in Molecular syndromology (01.03.2013)
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Mowat-Wilson syndrome: the first two Malaysian cases
Balasubramaniam, S, Keng, W T, Ngu, L H, Michel, L G, Irina, G
Published in Singapore medical journal (01.03.2010)
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Published in Singapore medical journal (01.03.2010)
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A3243G mitochondrial mutation associated with polymicrogyria
Keng, WT, Pilz, DT, Minns, B, FitzPatrick, DR
Published in Developmental medicine and child neurology (01.10.2003)
Published in Developmental medicine and child neurology (01.10.2003)
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Molecular analysis of fragile X syndrome (FXS) among Malaysian patients with developmental disability
Ali, E Z, Yakob, Y, Md Desa, N, Ishak, T, Zakaria, Z, Ngu, L K, Keng, W T
Published in Malaysian journal of pathology (01.08.2017)
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Published in Malaysian journal of pathology (01.08.2017)
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Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
Williamson, Kathleen A., Hever, Ann M., Rainger, Joe, Rogers, R. Curtis, Magee, Alex, Fiedler, Zdenek, Keng, Wee Teik, Sharkey, Freddie H., McGill, Niolette, Hill, Clare J., Schneider, Adele, Messina, Mario, Turnpenny, Peter D., Fantes, Judy A., van Heyningen, Veronica, FitzPatrick, David R.
Published in Human molecular genetics (01.05.2006)
Published in Human molecular genetics (01.05.2006)
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Journal Article
A3243G mitochondrial mutation associated with polymicrogyria
Keng, WT, Pilz, DT, Minns, B, Patrick, DR Fitz
Published in Developmental medicine and child neurology (01.10.2003)
Published in Developmental medicine and child neurology (01.10.2003)
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Journal Article
Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome
Williamson, Kathleen A., Hever, Ann M., Rainger, Joe, Rogers, R. Curtis, Magee, Alex, Fiedler, Zdenek, Keng, Wee Teik, Sharkey, Freddie H., McGill, Niolette, Hill, Clare J., Schneider, Adele, Messina, Mario, Turnpenny, Peter D., Fantes, Judy A., van Heyningen, Veronica, FitzPatrick, David R.
Published in Human molecular genetics (15.06.2006)
Published in Human molecular genetics (15.06.2006)
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Effective monosomy or trisomy of chromosome band 2q37.3 due to the unbalanced segregation of a 2;11 translocation
Batstone, Paul J., Simpson, Sheila, Bonthron, David T., Keng, Wee T., Hamilton, Doreen, Forsyth, Linda, Sales, Mark, Pratt, Norman, Goudie, David
Published in American journal of medical genetics. Part A (30.04.2003)
Published in American journal of medical genetics. Part A (30.04.2003)
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Journal Article
A balanced reciprocal translocation in a case of hypomelanosis of Ito with confirmation of mosaicism using buccal cell interphase FISH
Keng, W T, Harewood, L, Grace, E, Paxton, C, Lam, W W K, Fitzpatrick, D R
Published in American journal of medical genetics. Part A (15.05.2006)
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Published in American journal of medical genetics. Part A (15.05.2006)
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