K J Hsiao - JoVE Visualize

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Human Genetics|September 15, 2000

Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutationW L Hwu, P J Wang, K J Hsiao, et al.

Taiwan Yi Xue Hui Za Zhi. Journal of the Formosan Medical Association|July 1, 1989

Abnormal thyroid function and hypercholesterolemia in a case of acute intermittent porphyriaJ W Shiue, F Y Lee, K J Hsiao, et al.

Human Mutation|July 5, 2001

Identification of three novel 6-pyruvoyl-tetrahydropterin synthase gene mutations (226C>T, IVS3+1G>A, 116-119delTGTT) in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiencyT T Liu, Y H Chang, S H Chiang, et al.

American Journal of Medical Genetics|February 21, 1997

Further evidence of no association between Ser9Gly polymorphism of dopamine D3 receptor gene and schizophreniaC H Chen, M Y Liu, F C Wei, et al.

Human Genetics|February 1, 1989

Study of restriction fragment length polymorphisms at the human phenylalanine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in ChineseS H Chen, K J Hsiao, L H Lin, et al.

Molecular Psychiatry|December 1, 1999

Detection of Borna disease virus RNA from peripheral blood cells in schizophrenic patients and mental health workersC H Chen, Y L Chiu, C K Shaw, et al.

Journal of Inherited Metabolic Disease|October 16, 2009

Novel mutation affecting the pterin-binding site of PTS gene and review of PTS mutations in Thai patients with 6-pyruvoyltetrahydropterin synthase deficiencyN Vatanavicharn, C Kuptanon, S Liammongkolkul, et al.

Human Mutation|April 29, 1998

Identification of a novel point mutation (S65T) in alpha-galactosidase A gene in Chinese patients with Fabry disease. Mutations in brief no. 169. OnlineC H Chen, P W Shyu, S J Wu, et al.

American Journal of Medical Genetics|November 22, 1996

Identification of a BglI polymorphism of catechol-O-methyltransferase (COMT) gene, and association study with schizophreniaC H Chen, Y R Lee, M Y Liu, et al.

Human Genetics|May 1, 1994

Absence of FMR-1 gene expression can be detected with RNA extracted from dried blood specimensJ T Pai, S F Tsai, C J Horng, et al.

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Showing results (31-40 of 55) with videos related to

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Pageof 6

Human Genetics|September 15, 2000

Dopa-responsive dystonia induced by a recessive GTP cyclohydrolase I mutationW L Hwu, P J Wang, K J Hsiao, et al.

Taiwan Yi Xue Hui Za Zhi. Journal of the Formosan Medical Association|July 1, 1989

Abnormal thyroid function and hypercholesterolemia in a case of acute intermittent porphyriaJ W Shiue, F Y Lee, K J Hsiao, et al.

Human Mutation|July 5, 2001

Identification of three novel 6-pyruvoyl-tetrahydropterin synthase gene mutations (226C>T, IVS3+1G>A, 116-119delTGTT) in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiencyT T Liu, Y H Chang, S H Chiang, et al.

American Journal of Medical Genetics|February 21, 1997

Further evidence of no association between Ser9Gly polymorphism of dopamine D3 receptor gene and schizophreniaC H Chen, M Y Liu, F C Wei, et al.

Human Genetics|February 1, 1989

Study of restriction fragment length polymorphisms at the human phenylalanine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in ChineseS H Chen, K J Hsiao, L H Lin, et al.

Molecular Psychiatry|December 1, 1999

Detection of Borna disease virus RNA from peripheral blood cells in schizophrenic patients and mental health workersC H Chen, Y L Chiu, C K Shaw, et al.

Journal of Inherited Metabolic Disease|October 16, 2009

Novel mutation affecting the pterin-binding site of PTS gene and review of PTS mutations in Thai patients with 6-pyruvoyltetrahydropterin synthase deficiencyN Vatanavicharn, C Kuptanon, S Liammongkolkul, et al.

Human Mutation|April 29, 1998

Identification of a novel point mutation (S65T) in alpha-galactosidase A gene in Chinese patients with Fabry disease. Mutations in brief no. 169. OnlineC H Chen, P W Shyu, S J Wu, et al.

American Journal of Medical Genetics|November 22, 1996

Identification of a BglI polymorphism of catechol-O-methyltransferase (COMT) gene, and association study with schizophreniaC H Chen, Y R Lee, M Y Liu, et al.

Human Genetics|May 1, 1994

Absence of FMR-1 gene expression can be detected with RNA extracted from dried blood specimensJ T Pai, S F Tsai, C J Horng, et al.

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