File:Critical region of Angelman Syndrome on chromosome 15.png
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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|current||07:30, 1 October 2011||591 × 576 (356 KB)||Z3291643||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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