Orphanet Journal of Rare Diseases

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Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome

Maria C Roberti*, Cecilia Surace, Maria C Digilio, Gemma D'Elia, Pietro Sirleto, Rossella Capolino, Antonietta Lombardo, Anna C Tomaiuolo, Stefano Petrocchi and Adriano Angioni

Orphanet Journal of Rare Diseases 2011, 6:17 doi:10.1186/1750-1172-6-17

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