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1. S02. Delineation of a recognisable phenotype of interstitial deletion 3 (q22.3q25.1) in a case with previously unreported truncus arteriosus

2. S2. APPLICATION OF ARRAY-CGH FOR THE DETECTION OF SUBMICROSCOPIC CHROMOSOMAL IMBALANCES IN 400 CASES OF CHILDREN WITH IDIOPATHIC MENTAL RETARDATION AND CONGENITAL MALFORMATIONS

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