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Molecular analysis and prenatal diagnosis of peroxisome biogenesis disorders
Molecular analysis and prenatal diagnosis of peroxisome biogenesis disorders
Paper
Digital
博士論文
障害者向け資料あり
張忠義 [著]
[張忠義]
[2000]
<UT51-2000-N668>
Available online
National Diet Library
Molecular analysis and prenatal diagnosis of peroxisome biogenesis disorders
(1) Genomic stucture and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders (2) Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells
Molecular analysis and prenatal diagnosis of peroxisome biogenesis disorders (1) Genomic stucture and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders (2) Prenatal diagnosis of peroxisome biogenesis disorders by means of immunofluorescence staining of cultured chorionic villous cells
Paper
博士論文
張, 忠義
2000-03-24
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