Early onset intellectual disability in chromosome 22q11.2 deletion syndrome
Chromosome 22q11.2 deletion syndrome, or DiGeorge syndrome, or velocardiofacial syndrome, is one of the most common multiple anomaly syndromes in humans. This syndrome is commonly caused by a microdelection from chromosome 22 at band q11.2. Although this genetic disorder may reflect several clinical...
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| Langue: | English |
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Sociedad Chilena de Pediatría
2015
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| Accès en ligne: | http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062015000400010 |
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