3q27.3 microdeletional syndrome: a recognisable clinical entity associating dysmorphic features, marfanoid habitus, intellectual disability and psychosis with mood disorder.


BACKGROUND Since the advent of array-CGH, numerous new microdeletional syndromes have been delineated while others remain to be described. Although 3q29 subtelomeric deletion is a well-described syndrome, there is no report on 3q interstitial deletions. METHODS We report for the first time seven patients with interstitial deletions at the 3q27.3q28 locus… (More)
DOI: 10.1136/jmedgenet-2013-101939



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