Jump to main content
文書・図像類

読字障害の責任遺伝子の特定 : Williams症候群をモデルとして

Icons representing 文書・図像類

読字障害の責任遺伝子の特定 : Williams症候群をモデルとして

Material type
文書・図像類
Author
柳橋, 達彦
Publisher
-
Publication date
2010
Material Format
Digital
Capacity, size, etc.
-
NDC
-
View All

Notes on use

Note (General):

type:textWilliams症候群は、心奇形、特有の顔貌、認知機能障害を呈する。7q11.23領域の1.4-1.6Mbのヘミ接合体欠失で生じ、その欠失範囲と認知機能障害の重症度との関係が注目されている。本研究は、Williams症候群患者の欠失範囲をアレイ比較ゲノムハイブリダイゼーション法で解...

Related materials as well as pre- and post-revision versions

科研費研究者番号 : 10383770

Search by Bookstore

Holdings of Libraries in Japan

This page shows libraries in Japan other than the National Diet Library that hold the material.

Please contact your local library for information on how to use materials or whether it is possible to request materials from the holding libraries.

other

  • Keio Associated Repository of Academic resources

    Digital
    You can check the holdings of institutions and databases with which Institutional Repositories DataBase(IRDB)(Institutional Repository) is linked at the site of Institutional Repositories DataBase(IRDB)(Institutional Repository).

Bibliographic Record

You can check the details of this material, its authority (keywords that refer to materials on the same subject, author's name, etc.), etc.

Digital

Material Type
文書・図像類
Author/Editor
柳橋, 達彦
Author Heading
Publication Date
2010
Publication Date (W3CDTF)
2010
Alternative Title
ドクジ ショウガイ ノ セキニン イデンシ ノ トクテイ : Williams ショウコウグン オ モデル ト シテ
Dokuji shogai no sekinin idenshi no tokutei : Williams shokogun o moderu to shite
Identification of causative genes for reading disability in Williams syndrome
Periodical title
科学研究費補助金研究成果報告書
Text Language Code
jpn