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非侵襲的出生前遺伝子学的検査(新型出生前診断)における課題と問題点における考察
https://doi.org/10.57314/00000038
https://doi.org/10.57314/000000380baf6a3c-2d8e-403a-a636-c8123ac591cd
名前 / ファイル | ライセンス | アクション |
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38T_Funato.pdf (952.0 kB)
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Item type | 学術雑誌論文 / Journal Article(1) | |||||
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公開日 | 2015-04-20 | |||||
タイトル | ||||||
言語 | ja | |||||
タイトル | 非侵襲的出生前遺伝子学的検査(新型出生前診断)における課題と問題点における考察 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Clinical and Societal Issues Surrounding New, Non-Invasive Prenatal Genetic Testing Methods | |||||
言語 | ||||||
言語 | jpn | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | non-invasiveprenatalgenetictesting(非侵襲的出生前遺伝学的検査) | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | prenatalscreening(出生前診断) | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | trisomy21(21トリソミー) | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | trisomy18(18トリソミー) | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | trisomy13(13トリソミー) | |||||
キーワード | ||||||
言語 | ja | |||||
主題Scheme | Other | |||||
主題 | geneticcounseling(遺伝カウンセリング) | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | non-invasiveprenatalgenetictesting | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | prenatalscreening | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | trisomy21 | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | trisomy18 | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | trisomy13 | |||||
キーワード | ||||||
言語 | en | |||||
主題Scheme | Other | |||||
主題 | geneticcounseling | |||||
資源タイプ | ||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
資源タイプ | journal article | |||||
ID登録 | ||||||
ID登録 | 10.57314/00000038 | |||||
ID登録タイプ | JaLC | |||||
著者 |
舩渡, 忠男
× 舩渡, 忠男 |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | The invasive procedures amniocentesis and chorionic villus sampling are routinelyapplied in pregnancies at risk for fetal genetic disorders and the results obtained are the goldstandard for prenatal diagnosis. In recently, the field of prenatal genetic testing has explodedwith new non-invasive genetic technologies. These recent technological advances in prenataldiagnosis : interrogation of the fetal genome in increasingly high resolution and the developmentof non-invasive methods of fetal testing using cell-free DNA in maternal plasma. In thispaper, it has examined the sequencing technologies that provide the framework for non-invasiveprenatal testing( NIPT) and review the major studies published. This review summarizesrecent developments in the field of non-invasive prenatal diagnosis through the use of cellfreefetal nucleic acids in maternal circulation during pregnancy and provides an overview of thepossibilities for future clinical applications. This review summarizes recent work in this fieldand discusses the integration of these new technologies into the clinic and society. | |||||
言語 | en | |||||
書誌情報 |
ja : 東北福祉大学研究紀要 en : Bulletin of Tohoku Fukushi University 巻 38, p. 185-197, 発行日 2014-03-20 |
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出版者 | ||||||
言語 | ja | |||||
出版者 | 東北福祉大学 | |||||
ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 1340-5012 | |||||
書誌レコードID | ||||||
収録物識別子タイプ | NCID | |||||
収録物識別子 | AN10437669 | |||||
論文ID(NAID) | ||||||
識別子タイプ | NAID | |||||
関連識別子 | 40020302306 |