Spectrum of hypermethioninemia in Taiwan
スポンサーリンク
概要
- 論文の詳細を見る
- 2007-10-23
著者
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CHIEN Yin-Hsiu
Department of Medical Genetics, National Taiwan University Hospital, National Taiwan University
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Lee Ni-chung
Department Of Pediatrics And Medical Genetics National Taiwan University Hospital
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HWU Wuh-Liang
Department of Pediatrics, College of Medicine, National Taiwan University Hospital
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Hwu Wuh-liang
Department Of Pediatrics And Medical Genetics National Taiwan University Hospital
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Hwu Wuh-liang
Department Of Medical Genetics College Of Medicine National Taiwan University
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Chien Yin-hsiu
Department Of Pediatrics And Medical Genetics National Taiwan University Hospital
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Chien Yin-hsiu
Department Of Medical Genetics National Taiwan University Hospital National Taiwan University
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MUDD S.
NIMH, Bethesda
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HUANG Ai-Chu
Department of Medical Genetics and Pediatrics, National Taiwan University Hospital
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Huang Aichu
Department Of Pediatrics And Medical Genetics National Taiwan University Hospital
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Mudd S.
Nimh Bethesda
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Chien Yin-hsiu
Department Of Medical Genetics National Taiwan University Hospital
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Hwu Wuh-liang
Department Of Medical Genetics National Taiwan University Hospital
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Hwu Wuh-liang
Department Of Medical Genetics And Pediatrics National Taiwan University Hospital
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CHIEN Yin-Hsiu
Department of Medical Genetics and Pediatrics, National Taiwan University Hospital
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LEE Ni-Chung
Department of Medical Genetics and Pediatrics, National Taiwan University Hospital
関連論文
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- The controversy regarding diagnostic criteria for early myoclonic encephalopathy
- Spectrum of hypermethioninemia in Taiwan
- Changing outcome in inborn errors after newborn screening
- Phenotypes and genotypes of hyperphenylalaninemia in Taiwan
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- Glucose-6-phosphatase gene mutations in Taiwan Chinese patients with glycogen storage disease type Ia
- Hyperammonemia and positive allopurinol test in hyperinsulinism-hyperammonemia syndrome : Taiwanese case report
- Spectrum of hypermethioninemia in Taiwan
- Changing outcome in inborn errors after newborn screening
- The Impact of Tandem Mass Technology on the Management of Inborn Errors in Taiwan
- Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer
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- Anti-rhGAA antibody formation in Chinese Pompe disease infants underwent enzyme replacement therapy
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