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- W2571947982 abstract "The rearrangements between chromosome Y and 22, and chromosome 15 and 22 in patients with Velocardiofacial and Prader-Willi syndromes were observed by karyotyping. The deletion of TUPLE1 and SNRPN genes were also detected by Fluorescence in situ Hybridization. It can be concluded that the rearrangements were unbalance translocations. Therefore, the combination of karyotyping and molecular cytogenetic tests should be recommended to identify submicroscopic chromosome deletion and/or unbalanced rearrangement." @default.
- W2571947982 created "2017-01-26" @default.
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- W2571947982 date "2013-01-01" @default.
- W2571947982 modified "2023-09-23" @default.
- W2571947982 title "การจ าแนกการเกิดทรานสโลเกชั นของโครโมโซมที่มองไม่ห็ใต้ล้งใน ผู ้่ วยในกลุ ่อาการ microdeletion Submicroscopic identification of chromosomal translocation in patients with microdeletion syndromes" @default.
- W2571947982 cites W2078637082 @default.
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- W2571947982 hasPublicationYear "2013" @default.
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