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https://doi.org/10.1136/archdischild-2018-314779
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Cite Journal: Archives of Disease in Childhood |  Publication Date: Apr 7, 2018 |
 Citations: 20 |
ObjectiveThe 22q11.2 deletion syndrome (22q11.2DS) is the most common microdeletion syndrome in humans. It is characterised by wide phenotypic variability, including congenital heart disease (CHD), immunodeficiency and scoliosis. However, little...
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