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Human Molecular Genetics|January 1, 1995
Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analysesD G Monckton, L J Wong, T Ashizawa, et al.
Molecular Genetics and Metabolism|February 13, 2001
Molecular genetics of glycogen-storage disease type 1a in Chinese patients of TaiwanL J Wong, W L Hwu, P Dai, et al.
Clinical Neuropathology|April 10, 2009
A novel homozygous SCO2 mutation, p.G193S, causing fatal infantile cardioencephalomyopathyB C Mobley, G M Enns, L-J Wong, et al.
American Journal of Medical Genetics|August 3, 2001
Novel SNP at the common primer site of exon IIIa of FGFR2 gene causes error in molecular diagnosis of craniosynostosis syndromeL J Wong, T J Chen, P Dai, et al.
European Journal of Pediatrics|September 4, 1998
Mitochondrial DNA deletion with Kearns Sayre syndrome in a child with Addison diseaseR G Boles, T Roe, D Senadheera, et al.
Prenatal Diagnosis|October 20, 2000
A novel mutation detected by temporal temperature gradient gel electrophoresis led to the confirmative prenatal diagnosis of a Hispanic CF familyL J Wong, J Wang, M Woo, et al.
Molecular Genetics and Metabolism|June 23, 1998
Molecular and biochemical basis of galactosemiaB B Wang, Y K Xu, W G Ng, et al.
Experientia|May 15, 1990
Inhibition of in vitro RNA synthesis by hycanthone, oxamniquine and praziquantelL J Wong, G C Tsao, J I Bruce, et al.
Human Genetics|October 6, 1998
Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase geneL J Wong, M H Liang, W L Hwu, et al.
Biochemistry|March 8, 1977
Galactose-1-phosphate uridylyltransferase: isolation and properties of a uridylyl-enzyme intermediateL J Wong, K F Sheu, S L Lee, et al.
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