C H Chen|K J Hsiao - JoVE Visualize

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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 Hsiao

Molecular Psychiatry|July 8, 1999

Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from TaiwanM T Tsai, C K Shaw, K J Hsiao, et al.

Human Genetics|July 1, 1996

Chinese achondroplasia is also defined by recurrent G380R mutations of the fibroblast growth factor receptor-3 geneD M Niu, K J Hsiao, N H Wang, et al.

European Journal of Pediatrics|October 1, 1986

A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screeningK J Hsiao, C H Chen, P C Chiu, et al.

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

Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese childrenK J Hsiao, C H Chen, T T Liu, et al.

Psychiatric Genetics|April 1, 1997

Lack of allelic association between 102T/C polymorphism of serotonin receptor type 2A gene and schizophrenia in ChineseC H Chen, Y R Lee, F C Wei, 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.

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.

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.

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Pageof 138

The British Journal of Psychiatry : the Journal of Mental Science|August 1, 1989

A Chinese classic phenylketonuria manifested as autismC H Chen, K J Hsiao

Molecular Psychiatry|July 8, 1999

Genetic association study of a polymorphic CAG repeats array of calcium-activated potassium channel (KCNN3) gene and schizophrenia among the Chinese population from TaiwanM T Tsai, C K Shaw, K J Hsiao, et al.

Human Genetics|July 1, 1996

Chinese achondroplasia is also defined by recurrent G380R mutations of the fibroblast growth factor receptor-3 geneD M Niu, K J Hsiao, N H Wang, et al.

European Journal of Pediatrics|October 1, 1986

A Chinese family with phenylketonuria and maternal phenylketonuria detected by family screeningK J Hsiao, C H Chen, P C Chiu, et al.

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

Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese childrenK J Hsiao, C H Chen, T T Liu, et al.

Psychiatric Genetics|April 1, 1997

Lack of allelic association between 102T/C polymorphism of serotonin receptor type 2A gene and schizophrenia in ChineseC H Chen, Y R Lee, F C Wei, 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.

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.

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.

Pageof 138