File:Critical region of Angelman Syndrome on chromosome 15.png: Difference between revisions
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==Critical region of Angelman Syndrome on chromosome 15== | |||
Prader Willi & Angelman's syndromes - probes | Prader Willi & Angelman's syndromes - probes | ||
Human chromosome highlighted by fluorescent probes | Human chromosome highlighted by fluorescent probes | ||
Revision as of 12:31, 13 October 2011
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, April 24) 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
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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| current | 07:30, 1 October 2011 |  | 591 × 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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