File:FISH using HIRA probe.jpeg: Difference between revisions

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(An image obtained with Fluorescent in situ hybridisation (FISH) using a HIRA probe. The orange signal shows the locus at 22q11.2 (showing one copy), the green signal shows chromosome 22q13 as a control (showing 2 copies). The absence of two orange signals)
 
 
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==Image Information==
An image obtained with Fluorescent in situ hybridisation (FISH) using a HIRA probe. The orange signal shows the locus at 22q11.2 (showing one copy), the green signal shows chromosome 22q13 as a control (showing 2 copies). The absence of two orange signals illustrates a deletion of a locus at 22q11.2, which is characteristic of DiGeorge Syndrome.


===Reference===
{{#pmid:20396437}}


An image obtained with Fluorescent in situ hybridisation (FISH) using a HIRA probe. The orange signal shows the locus at 22q11.2 (showing one copy), the green signal shows chromosome 22q13 as a control (showing 2 copies). The absence of two orange signals illustrates a deletion of a locus at 22q11.2, which is characteristic of DiGeorge Syndrome.  
====Copyright====
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Image obtained from:
===Assessment===
"Psychotic features as the first manifestation of 22q11.2 deletion syndrome".
+ Relevant research image to group topic.
Kook SD, An SK, Kim KR, Kim WJ, Lee E, Namkoong K.
+ Reference and copyright information included. Not using aotoformat reference as shown below.
Psychiatry Investig. 2010 Mar;7(1):72-4. Epub 2010 Feb 19.
+/- Legend is descriptive of image, but appears to be original without any student learning interpretation or simplification. For example, what is a HIRA probe?
PMID: 20396437 [PubMed]
- Missing student disclaimer.


 
===Reference===
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
{{#pmid:20396437}}

Latest revision as of 10:54, 18 December 2018

Image Information

An image obtained with Fluorescent in situ hybridisation (FISH) using a HIRA probe. The orange signal shows the locus at 22q11.2 (showing one copy), the green signal shows chromosome 22q13 as a control (showing 2 copies). The absence of two orange signals illustrates a deletion of a locus at 22q11.2, which is characteristic of DiGeorge Syndrome.

Reference

Kook SD, An SK, Kim KR, Kim WJ, Lee E & Namkoong K. (2010). Psychotic features as the first manifestation of 22q11.2 deletion syndrome. Psychiatry Investig , 7, 72-4. PMID: 20396437 DOI.

Copyright

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Assessment

+ Relevant research image to group topic. + Reference and copyright information included. Not using aotoformat reference as shown below. +/- Legend is descriptive of image, but appears to be original without any student learning interpretation or simplification. For example, what is a HIRA probe? - Missing student disclaimer.

Reference

Kook SD, An SK, Kim KR, Kim WJ, Lee E & Namkoong K. (2010). Psychotic features as the first manifestation of 22q11.2 deletion syndrome. Psychiatry Investig , 7, 72-4. PMID: 20396437 DOI.

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current13:20, 5 October 2011Thumbnail for version as of 13:20, 5 October 2011479 × 222 (10 KB)Z3288196 (talk | contribs) An image obtained with Fluorescent in situ hybridisation (FISH) using a HIRA probe. The orange signal shows the locus at 22q11.2 (showing one copy), the green signal shows chromosome 22q13 as a control (showing 2 copies). The absence of two orange signa

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