Mendeley出力
＜図書＞
Molecular diagnosis of genetic diseases
| 責任表示 | edited by Rob Elles |
|---|---|
| シリーズ | Methods in molecular medicine / John M. Walker, series editor |
| データ種別 | 図書 |
| 出版情報 | Totowa, N.J. : Humana Press , c1996 |
| 本文言語 | 英語 |
| 大きさ | xi, 356 p. : ill. ; 23 cm |
| 概要 | Expert clinical investigators present their best and most reliable methods for the molecular diagnosis of common genetic disorders. The methods-organized by disease or diagnostic area-are robust and ...eproducible. They contain not only essential day-to-day benchtop wisdom and instruction, but also offer possibilities for introducing new molecular genetic diagnostic tests, as well as invaluable advice on controls, quality standards, and interpretation. Among the genetic diseases discussed are Duchenne/Becker muscular dystrophy, familial adenomatous polyposis, X-chromosome inactivation, Prader-Willi and Angelman syndromes, Huntington's disease, myotonic dystrophy, fragile X disease, cystic fibrosis, familial hypochloresterolemia, and the hemoglobinopathies. 続きを見る |
| 電子版へのリンク | https://hdl.handle.net/2324/6976908 |
所蔵情報
| 状態 | 巻次 | 所蔵場所 | 請求記号 | 刷年 | 文庫名称 | 資料番号 | コメント | 予約・取寄 | 複写申込 | 自動書庫 |
|---|---|---|---|---|---|---|---|---|---|---|
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医学図 3F 保存・図書 | QZ 50/M 718/1996 | 1996 |
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042221998000632 |
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書誌詳細
| 一般注記 | Includes bibliographical references and index |
|---|---|
| 著者標目 | Elles, Rob |
| 件 名 | LCSH:Genetic disorders -- Molecular diagnosis -- Laboratory manuals
全ての件名で検索
MESH:Hereditary Diseases -- diagnosis 全ての件名で検索 MESH:Genetic Screening MESH:Genetic Techniques |
| 分 類 | LCC:RB155.6 NLM:QZ 50 M71835 1996 DC20:616/.042 |
| 書誌ID | 1000276903 |
| ISBN | 0896033465 |
| NCID | BA28719510 |
| 巻冊次 | ISBN:0896033465 |
| 登録日 | 2009.09.11 |
| 更新日 | 2017.02.18 |