{"created":"2023-06-20T16:59:27.858062+00:00","id":18571,"links":{},"metadata":{"_buckets":{"deposit":"c1893b8e-e23a-42cc-802e-1f168f2dc629"},"_deposit":{"created_by":3,"id":"18571","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"18571"},"status":"published"},"_oai":{"id":"oai:twinkle.repo.nii.ac.jp:00018571","sets":["140:1307:1308:1956:1963"]},"author_link":["266323","266324"],"item_10001_alternative_title_1":{"attribute_name":"別タイトル","attribute_value_mlt":[{"subitem_alternative_title":"Clinical Study of the Deletion of Chromosome 22q11"}]},"item_10001_biblio_info_7":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2001-10-25","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"9/10","bibliographicPageEnd":"727","bibliographicPageStart":"721","bibliographicVolumeNumber":"71","bibliographic_titles":[{"bibliographic_title":"東京女子医科大学雑誌"}]}]},"item_10001_creator_2":{"attribute_name":"著者名","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"門間, 和夫"}],"nameIdentifiers":[{}]}]},"item_10001_date_25":{"attribute_name":"受付日付","attribute_value_mlt":[{"subitem_date_issued_datetime":"2010-08-10","subitem_date_issued_type":"Created"}]},"item_10001_description_5":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"The deletion of chromosome 22q11 causes conotruncal anomaly face syndrome. This syndrome was recognized in our Department since mid 1970s. Its chromosomal base was established in 1992. Since then, we have identified 200 patients with fluorescence in-situ hybridization. The most prevalent disease associated with the deletion is tetralogy of Fallot. Tetralogy with the deletion is characteristically associated with anomalies of the aortic arch, ductus arteriosus and pulmonary artery. The prevalence of the deletion is especially high in patients with type B interruption of the aortic arch, tetralogy of Fallot with pulmonary atresia and major aorto-pulmonary collateral arteries, and truncus arteriosus. Mild but progressive mental retardation is common. Schizophrenia develops in some 15% of the adolescent patients.","subitem_description_type":"Abstract"}]},"item_10001_full_name_3":{"attribute_name":"著者別名","attribute_value_mlt":[{"nameIdentifiers":[{"nameIdentifier":"266324","nameIdentifierScheme":"WEKO"}],"names":[{"name":"MOMMA, Kazuo"}]}]},"item_10001_publisher_8":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"東京女子医科大学学会"}]},"item_10001_source_id_11":{"attribute_name":"NCID","attribute_value_mlt":[{"subitem_source_identifier":"AN00161368","subitem_source_identifier_type":"NCID"}]},"item_10001_source_id_9":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0040-9022","subitem_source_identifier_type":"ISSN"}]},"item_10001_text_35":{"attribute_name":"著者所属","attribute_value_mlt":[{"subitem_text_value":"東京女子医科大学医学部循環器小児科学"}]},"item_10001_version_type_20":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_970fb48d4fbd8a85","subitem_version_type":"VoR"}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-03-27"}],"displaytype":"detail","filename":"KJ00006020030.pdf","filesize":[{"value":"1.0 MB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"KJ00006020030.pdf","url":"https://twinkle.repo.nii.ac.jp/record/18571/files/KJ00006020030.pdf"},"version_id":"86943e7e-57b3-4e69-a07e-27328ade4517"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"jpn"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"染色体22q11欠失症の臨床","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"染色体22q11欠失症の臨床"}]},"item_type_id":"10001","owner":"3","path":["1963"],"pubdate":{"attribute_name":"公開日","attribute_value":"2010-08-10"},"publish_date":"2010-08-10","publish_status":"0","recid":"18571","relation_version_is_last":true,"title":["染色体22q11欠失症の臨床"],"weko_creator_id":"3","weko_shared_id":-1},"updated":"2023-06-20T22:26:46.867778+00:00"}