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Singapore Medical Journal|June 22, 2005
The spectrum of beta-globin gene mutations in children with beta-thalassaemia major from Kota Kinabalu, Sabah, MalaysiaM K Thong, T L SooThe Medical Journal of Malaysia|September 24, 2011
Partial deletion 9p syndrome in Malaysian childrenH B Chew, M K ThongSingapore Medical Journal|June 1, 1996
Two brothers in a Malaysian family with X-linked lymphoproliferative disease--a case reportA Hany, M K Thong, H P LinThe Medical Journal of Malaysia|December 1, 1996
Supernumerary chromosomes in mosaic Turner syndromeM K Thong, V Manonmani, I S NorlasiahAnnals of the Academy of Medicine, Singapore|January 1, 1996
Molecular heterogeneity of beta-thalassaemia in Malaysia: a practical approach to diagnosisM K Thong, H Y Law, I S NgAnnals of Human Biology|August 13, 2005
A population-based study of birth defects in MalaysiaM K Thong, J J Ho, N N KhatijahSingapore Medical Journal|January 4, 1998
Distal renal tubular acidosis and hereditary elliptocytosis in a single familyM K Thong, A A Tan, H P LinAmerican Journal of Medical Genetics|August 22, 2000
Acampomelic campomelic dysplasia with SOX9 mutationM K Thong, G Scherer, K Kozlowski, et al.Annals of the Academy of Medicine, Singapore|July 1, 1997
Group B streptococcus: maternal carriage rate and early neonatal septicaemiaC T Lim, M K Thong, N Parasakthi, et al.Journal of Inherited Metabolic Disease|January 24, 2009
Congenital disorder of glycosylation type Ia in a Malaysian family: clinical outcome and description of a novel PMM2 mutationM K Thong, M Fietz, C Nicholls, et al.Pageof 3