File:Velocardiofacial syndrome with typical facies.jpg

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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

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Cite this page: Hill, M.A. (2024, April 24) 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

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© Dr Mark Hill 2024, UNSW Embryology ISBN: 978 0 7334 2609 4 - UNSW CRICOS Provider Code No. 00098G

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current23:26, 26 September 2011Thumbnail for version as of 23:26, 26 September 2011594 × 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 2011Thumbnail for version as of 23:24, 26 September 2011594 × 449 (171 KB)Z3308968 (talk | contribs)Reverted to version as of 14:40, 21 September 2011
23:23, 26 September 2011Thumbnail for version as of 23:23, 26 September 2011594 × 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 2011Thumbnail for version as of 00:40, 22 September 2011594 × 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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