Improved glycemia by hepatic insulin gene expression in insulin-dependent diabetes mellitus von Morral, Nuria, Dong, Hengjiang, MvEvoy, Robert, Meseck, Marcia, Woo, SavioL.C.

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SCREENING FOR PHENYLKETONURIA MUTATIONS BY DNA AMPLIFICATION WITH THE POLYMERASE CHAIN REACTION von Dilella, AnthonyG, Huang, Whei-Mei, Woo, SavioL.C.

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Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria von CHAKRABORTY, R, LIDSKY, A. S, DAIGER, S. P, GUTTLER, F, SULLIVAN, S, DILELLA, A. G, WOO, S. L. C

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A missense mutation, S349P, completely inactivates phenylalanine hydroxylase in North African Jews with phenylketonuria von WEINSTEIN, M, EISENSMITH, R. C, ABADIE, V, AVIGAD, S, LYONNET, S, SCHWARTZ, G, MUNNICH, A, WOO, S. L. C, SHILOH, Y

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PRENATAL DIAGNOSIS OF CLASSIC PHENYLKETONURIA BY DNA ANALYSIS von Lidsky, AlanS, Güttler, Flemming, Woo, SavioL.C

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Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy von DIANZANI, I, DEVOTO, M, ANGENEYDT, F, TREFZ, F. K, OKANO, Y, WOO, S. L. C, CAMASCHELLA, C, SAGLIO, G, FERRERO, G. B, CERONE, R, ROMANO, C, ROMEO, G, GIOVANNINI, M, RIVA, E

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POLYMORPHIC DNA HAPLOTYPES AT THE PHENYLALANINE HYDROXYLASE LOCUS IN PRENATAL DIAGNOSIS OF PHENYLKETONURIA von Daiger, StephenP, Chakraborty, Ranajit, Güttler, Flemming, Lidsky, AlanS, Koch, Richard, Woo, SavioL.C.

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PAH 399 GTA(Val)→GTT(Val), a new silent mutation found in the Chinese von HUANG, S.-Z, REN, Z.-R, ZENG, Y.-T, WOO, S. L. C

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