Lo WH - Search Results

1

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

Wang T, Okano Y, Eisensmith RC, Lo WH, Huang SZ, Zeng YT, Yuan LF, Liu SR, Woo SL. Wang T, et al. Among authors: lo wh. Genomics. 1992 May;13(1):230-1. doi: 10.1016/0888-7543(92)90229-l. Genomics. 1992. PMID: 1349576

2

Identification of three novel missense PKU mutations among Chinese.

Li J, Eisensmith RC, Wang T, Lo WH, Huang SZ, Zeng YT, Yuan LF, Liu SR, Woo SL. Li J, et al. Among authors: lo wh. Genomics. 1992 Jul;13(3):894-5. doi: 10.1016/0888-7543(92)90180-z. Genomics. 1992. PMID: 1639423

3

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

Wang T, Okano Y, Eisensmith RC, Lo WH, Huang SZ, Zeng YT, Woo SL. Wang T, et al. Among authors: lo wh. Am J Hum Genet. 1991 Mar;48(3):628-30. Am J Hum Genet. 1991. PMID: 1998345 Free PMC article.

4

Founder effect of a prevalent phenylketonuria mutation in the Oriental population.

Wang T, Okano Y, Eisensmith RC, Harvey ML, Lo WH, Huang SZ, Zeng YT, Yuan LF, Furuyama JI, Oura T, et al. Wang T, et al. Among authors: lo wh. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2146-50. doi: 10.1073/pnas.88.6.2146. Proc Natl Acad Sci U S A. 1991. PMID: 2006152 Free PMC article.

5

Missense mutations prevalent in Orientals with phenylketonuria: molecular characterization and clinical implications.

Wang T, Okano Y, Eisensmith RC, Lo WH, Huang SZ, Zeng YT, Yuan LF, Liu SR, Woo SL. Wang T, et al. Among authors: lo wh. Genomics. 1991 Jun;10(2):449-56. doi: 10.1016/0888-7543(91)90331-8. Genomics. 1991. PMID: 2071149

6

Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).

Daiger SP, Reed L, Huang SS, Zeng YT, Wang T, Lo WH, Okano Y, Hase Y, Fukuda Y, Oura T, et al. Daiger SP, et al. Among authors: lo wh. Am J Hum Genet. 1989 Aug;45(2):319-24. Am J Hum Genet. 1989. PMID: 2569272 Free PMC article.

7

Molecular genetics of phenylketonuria in Orientals: linkage disequilibrium between a termination mutation and haplotype 4 of the phenylalanine hydroxylase gene.

Wang T, Okano Y, Eisensmith R, Huang SZ, Zeng YT, Lo WH, Woo SL. Wang T, et al. Among authors: lo wh. Am J Hum Genet. 1989 Nov;45(5):675-80. Am J Hum Genet. 1989. PMID: 2816939 Free PMC article.

8

Phenylketonuria in China: identification and characterization of three novel nucleotide substitutions in the human phenylalanine hydroxylase gene.

Li J, Eisensmith RC, Wang T, Lo WH, Huang SZ, Zeng YT, Yuan LF, Liu SR, Woo SL. Li J, et al. Among authors: lo wh. Hum Mutat. 1994;3(3):312-4. doi: 10.1002/humu.1380030323. Hum Mutat. 1994. PMID: 8019568 No abstract available.

9

Molecular basis of PKU in China.

Lo WH, Wang T, Eisensmith R, Woo SL. Lo WH, et al. Chin Med Sci J. 1993 Sep;8(3):180-5. Chin Med Sci J. 1993. PMID: 8142636 No abstract available.

10

The same "TATA" box beta-thalassemia mutation in Chinese and US blacks: another example of independent origins of mutation.

Huang S, Wong C, Antonarakis SE, Ro-lien T, Lo WH, Kazazian HH Jr. Huang S, et al. Among authors: lo wh. Hum Genet. 1986 Oct;74(2):162-4. doi: 10.1007/BF00282081. Hum Genet. 1986. PMID: 3021607

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