File:Velocardiofacial syndrome with typical facies.jpg
Velocardiofacial_syndrome_with_typical_facies.jpg (594 × 449 pixels, file size: 171 KB, MIME type: image/jpeg)
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
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Cite this page: Hill, M.A. (2024, May 4) Embryology Velocardiofacial syndrome with typical facies.jpg. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/File:Velocardiofacial_syndrome_with_typical_facies.jpg
- © Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G
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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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