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(==Tetralogy of Fallot== An autopsied specimen has been opened through the anterior wall of the right ventricle to show the cardinal features of tetralogy of Fallot. ===Reference=== Bailliard and Anderson Orphanet Journal of Rare Diseases 2009 4:2 doi:)
 
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An autopsied specimen has been opened through the anterior wall of the right ventricle to show the cardinal features of tetralogy of Fallot.
An autopsied specimen has been opened through the anterior wall of the right ventricle to show the cardinal features of tetralogy of Fallot.
:'''Links:''' [[Cardiovascular_System_-_Tetralogy_of_Fallot|Tetralogy of Fallot]]
===Reference===
===Reference===
<pubmed>19144126</pubmed>| [http://www.ojrd.com/content/4/1/2 Orphanet J Rare Dis.]


Bailliard and Anderson Orphanet Journal of Rare Diseases 2009 4:2  doi:10.1186/1750-1172-4-2
Bailliard and Anderson Orphanet Journal of Rare Diseases 2009 4:2  doi:10.1186/1750-1172-4-2
====Copyright====
====Copyright====



Revision as of 23:49, 22 January 2013

Tetralogy of Fallot

An autopsied specimen has been opened through the anterior wall of the right ventricle to show the cardinal features of tetralogy of Fallot.


Links: Tetralogy of Fallot

Reference

<pubmed>19144126</pubmed>| Orphanet J Rare Dis.


Bailliard and Anderson Orphanet Journal of Rare Diseases 2009 4:2 doi:10.1186/1750-1172-4-2

Copyright

© 2009 Bailliard and Anderson; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

1750-1172-4-2-1.jpg

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current23:47, 22 January 2013Thumbnail for version as of 23:47, 22 January 2013700 × 873 (113 KB)Z8600021 (talk | contribs)==Tetralogy of Fallot== An autopsied specimen has been opened through the anterior wall of the right ventricle to show the cardinal features of tetralogy of Fallot. ===Reference=== Bailliard and Anderson Orphanet Journal of Rare Diseases 2009 4:2 doi:

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