File:Velocardiofacial syndrome with typical facies.jpg: Difference between revisions

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Velocardiofacial syndrome (VCFS) is an autosomal dominant condition which results from a deletion on the long arm of Chromosome 22 in the“q11”region (deletion22q11). It is the most common sub-microscopic deletion syndrome and is known to occur in 1 out of 2000 live births.

Reference

<pubmed>19884681</pubmed>| PMC2825080

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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	Date/Time	Dimensions	User	Comment
current	23:26, 26 September 2011	594 × 449 (171 KB)	Z3308968 (talk \| contribs)	===Reference=== <pubmed>19884681</pubmed>\| [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825080 PMC2825080] Velocardiofacial syndrome (VCFS) is an autosomal dominant condition which results from a deletion on the long arm of Chromosome 22 in the“q11�
	23:24, 26 September 2011	594 × 449 (171 KB)	Z3308968 (talk \| contribs)	Reverted to version as of 14:40, 21 September 2011
	23:23, 26 September 2011	594 × 449 (171 KB)	Z3308968 (talk \| contribs)	<pubmed>19884681</pubmed>\| [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825080 PMC2825080] This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduc
	00:40, 22 September 2011	594 × 449 (171 KB)	Z3308968 (talk \| contribs)	Velocardiofacial syndrome-An anomaly associated with cleft resulting from Chromosome 22q abnormality http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825080/ This is an open-access article distributed under the terms of the Creative Commons Attribution Lice

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-Velocardiofacial syndrome-An anomaly associated with cleft resulting from Chromosome 22q abnormality
+Velocardiofacial syndrome (VCFS) is an autosomal dominant condition which results from a deletion on the long arm of Chromosome 22 in the“q11”region (deletion22q11). It is the most common sub-microscopic deletion syndrome and is known to occur in 1 out of 2000 live births.
---[[User:S8600021|Mark Hill]] 10:37, 22 September 2011 (EST) fix this reference description as you have been shown in class, I have already corrected the citation format here, you should fix the other uploaded images.
 ===Reference===
 <pubmed>19884681</pubmed>| [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825080 PMC2825080]
-Velocardiofacial syndrome (VCFS) is an autosomal dominant condition which results from a deletion on the long arm of Chromosome 22 in the“q11”region (deletion22q11). It is the most common sub-microscopic deletion syndrome and is known to occur in 1 out of 2000 live births.
 This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.