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Wilson H.Y. Lo

Academy of Medical Sciences, United Kingdom

13

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197

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Linkage Studies of A Familial Spastic Paraplegia Pedigree from Tibet

1999 Chinese journal of medical genetics
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Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3

1997 Human Genetics
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Phenylketonuria in China: Identification and characterization of three novel nucleotide substitutions in the human phenylalanine hydroxylase gene

1994 Human Mutation
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Identification of three novel PKU mutations among Chinese : evidence for recombination or recurrent mutation at the PAH locus

1992 Genomics
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Identification of a novel phenylketonuria (PKU) mutation in the Chinese: further evidence for multiple origins of PKU in Asia.

1991 American Journal of Human Genetics
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Fragile X syndrome (Martin-Bell syndrome) in China.

1991 American Journal of Medical Genetics
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Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene

1989 American Journal of Human Genetics
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The same “TATA” box β-thalassemia mutation in Chinese and US blacks: another example of independent origins of mutation

1986 Human Genetics
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Phenotypic effects of inherited balanced translocation.

1982 American Journal of Medical Genetics
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Corresponding editor's column: Medical genetics in China

1981 American Journal of Medical Genetics
- Wilson H.Y. Lo
- Wu Min
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