File:FISH using HIRA probe.jpeg - Revision history

Z8600021: /* Reference and Copyright */

2018-12-18T00:54:46Z

Reference and Copyright

← Older revision		Revision as of 11:54, 18 December 2018
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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 illustrates a deletion of a locus at 22q11.2, which is characteristic of DiGeorge Syndrome.		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 ~~and Copyright~~==		===Reference===
	~~Image obtained from:"Psychotic features as the first manifestation of 22q11.2 deletion syndrome".~~		{{#pmid:20396437}}
	~~Kook SD, An SK, Kim KR, Kim WJ, Lee E, Namkoong K.~~
	~~Psychiatry Investig. 2010 Mar;7(1):72-4. Epub 2010 Feb 19.~~
	~~PMID~~: 20396437 ~~[PubMed]~~


			====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.		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.

Z8600021 at 00:30, 18 December 2018

2018-12-18T00:30:34Z

← Older revision		Revision as of 11:30, 18 December 2018
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	===Reference===		===Reference===
	~~<pubmed>~~20396437~~</pubmed>~~		{{#pmid:20396437}}

S8600021 at 06:40, 27 October 2011

2011-10-27T06:40:01Z

← Older revision		Revision as of 17:40, 27 October 2011
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	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.		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===
			<pubmed>20396437</pubmed>

Z3288729 at 09:46, 5 October 2011

2011-10-05T09:46:29Z

← Older revision		Revision as of 20:46, 5 October 2011
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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.		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.

	Image obtained from:		==Reference and Copyright==
	"Psychotic features as the first manifestation of 22q11.2 deletion syndrome".		Image obtained from:"Psychotic features as the first manifestation of 22q11.2 deletion syndrome".
	Kook SD, An SK, Kim KR, Kim WJ, Lee E, Namkoong K.		Kook SD, An SK, Kim KR, Kim WJ, Lee E, Namkoong K.
	Psychiatry Investig. 2010 Mar;7(1):72-4. Epub 2010 Feb 19.		Psychiatry Investig. 2010 Mar;7(1):72-4. Epub 2010 Feb 19.

Z3288196: 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

2011-10-05T03:20:35Z

New page

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.

Image obtained from:
"Psychotic features as the first manifestation of 22q11.2 deletion syndrome".
Kook SD, An SK, Kim KR, Kim WJ, Lee E, Namkoong K.
Psychiatry Investig. 2010 Mar;7(1):72-4. Epub 2010 Feb 19.
PMID: 20396437 [PubMed]

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.