ログイン
言語:

WEKO3

  • トップ
  • ランキング
To
lat lon distance
To

Field does not validate



インデックスリンク

インデックスツリー

メールアドレスを入力してください。

WEKO

One fine body…

WEKO

One fine body…

アイテム

  1. 広島大学の刊行物
  2. Hiroshima Journal of Medical Sciences
  3. 35巻3号

A Cytogenetic Study of Heavy Mental Retardates. III. A study on 114 karyotypes with banding techniques and incidence of chromosome abnormalities

https://hiroshima.repo.nii.ac.jp/records/2013098
https://hiroshima.repo.nii.ac.jp/records/2013098
6e7a8734-05f3-48b3-928b-d4c2e6ab5045
名前 / ファイル ライセンス アクション
HiroshimaJMedSci_35_271.pdf HiroshimaJMedSci_35_271.pdf (934.3 KB)
Item type デフォルトアイテムタイプ_(フル)(1)
公開日 2023-03-18
タイトル
タイトル A Cytogenetic Study of Heavy Mental Retardates. III. A study on 114 karyotypes with banding techniques and incidence of chromosome abnormalities
言語 en
作成者 KANATA, Suzue

× KANATA, Suzue

en KANATA, Suzue

Search repository
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
主題
主題Scheme Other
主題 Chromosome abnormality
主題
主題Scheme Other
主題 Mental retardation
主題
主題Scheme NDC
主題 490
内容記述
内容記述 A cytogenetic study was conducted on 114 cases with heavy mental retardation who were admitted to National Sanatorium Kamo Hospital and Hiroshima Prefectural Handicapped Children's Hospital. Of the 114 cases, 69 cases were males and 45 cases were females. These patients were classified into two groups according to clinical features: Group I of 58 cases with cerebral palsy and Group II of 56 cases with behavior disorders. Chromosome slides were prepared in accordance with the standard blood culture procedure. Karyotype analyses were made with the application of the conventional Giemsa staining and G-, C-, and Q-banding differential staining. Of these cases, 14 cases had abnormal karyotypes, showing an incidence of 12,3%. Of the 14 abnormal cases autosomal abnormalities were observed in 12 cases and sexchromosome abnormalities in 2 cases. And normal variations of no.1, 9, and Y chromosome were found in 11 cases. Out of the 58 cases with cerebral palsy belonging to Group I, 5 cases (8,6%) and out of 56 cases with behavior disorders belonging to Group II, 9 cases (16,1 %) had abnormal karyotypes. As a result of the chromosome analyses performed on available relatives of abnormal and normal cases with variations, one abnormal case and two of normal variations were found to be transmitted through the parental line.
言語 en
出版者
出版者 Hiroshima University School of Medicine
言語
言語 eng
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 departmental bulletin paper
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連情報
識別子タイプ PMID
関連識別子 3804787
収録物識別子
収録物識別子タイプ ISSN
収録物識別子 0018-2052
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA00664312
開始ページ
開始ページ 271
書誌情報 Hiroshima Journal of Medical Sciences
Hiroshima Journal of Medical Sciences

巻 35, 号 3, p. 271-277, 発行日 1986-09
旧ID 49929
戻る
0
views
See details
Views

Versions

Ver.1 2025-02-23 06:23:29.469183
Show All versions

Share

Mendeley Twitter Facebook Print Addthis

Cite as

エクスポート

OAI-PMH
  • OAI-PMH JPCOAR 2.0
  • OAI-PMH JPCOAR 1.0
  • OAI-PMH DublinCore
  • OAI-PMH DDI
Other Formats
  • JSON
  • BIBTEX

Confirm


Powered by WEKO3


Powered by WEKO3