File:Critical region of Angelman Syndrome on chromosome 15.png

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Critical region of Angelman Syndrome on chromosome 15

Prader Willi & Angelman's syndromes - probes Human chromosome highlighted by fluorescent probes that bind to specific sequences of DNA. In this FISH (fluorescence in situ hybridisation) study a probe (red) from the Prader Willi and Angelman's syndromes critical region (PSASCR) and a chromosome 15 centromere specific probe (green) show that the 15q.11>q13 duplication does not include the PWASCR.

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Cite this page: Hill, M.A. (2024, June 21) Embryology Critical region of Angelman Syndrome on chromosome 15.png. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Critical_region_of_Angelman_Syndrome_on_chromosome_15.png

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© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G

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current07:30, 1 October 2011Thumbnail for version as of 07:30, 1 October 2011591 × 576 (356 KB)Z3291643 (talk | contribs)Prader Willi & Angelman's syndromes - probes Human chromosome highlighted by fluorescent probes that bind to specific sequences of DNA. In this FISH (fluorescence in situ hybridisation) study a probe (red) from the Prader Willi and Angelman's syndromes c

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