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The British Journal of Psychiatry : the Journal of Mental Science|August 1, 1989
A Chinese classic phenylketonuria manifested as autismC H Chen, K J HsiaoHuman Genetics|September 1, 1996
Identification of a common 6-pyruvoyl-tetrahydropterin synthase mutation at codon 87 in Chinese phenylketonuria caused by tetrahydrobiopterin synthesis deficiencyT T Liu, K J HsiaoDiabetes Care|January 1, 1992
Community-based epidemiological study on diabetes in Pu-Li, TaiwanP Chou, H H Chen, K J HsiaoJournal of the Formosan Medical Association = Taiwan Yi Zhi|June 1, 1991
[Antenatal screening of maternal alpha-fetoprotein with dried-blood spot samples on filter paper]K J Hsiao, S Y Lee, H C ChuangHuman Genetics|February 24, 2001
A silent mutation induces exon skipping in the phenylalanine hydroxylase gene in phenylketonuriaH K Chao, K J Hsiao, T S SuThe Journal of Biological Chemistry|October 10, 1978
The role of ATP and divalent cations in the regulation of a cardiac phosphorylase phosphatase (phosphoprotein phosphatase) of Mr = 35,000K J Hsiao, A R Sandberg, H C LiHuman Genetics|April 1, 1990
Phenylketonuria mutation in Chinese haplotype 44 identical with haplotype 2 mutation in northern-European CaucasiansT F Tsai, K J Hsiao, T S SuBiochimica Et Biophysica Acta|August 11, 1977
Dissociation of phosphohistone phosphatases from canine heartK J Hsiao, W W Chan, H C LiJournal of Inherited Metabolic Disease|January 1, 1987
Pompe's disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activityC Y Lin, B Hwang, K J Hsiao, et al.Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|October 1, 1992
Community-based survey on blood pressure, blood biochemistry and dietary habits in Pu-Li, TaiwanP Chou, K J Hsiao, J W Lin, et al.Pageof 6