Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date

This paper was partially supported by Fundacion 1000 sobre Defectos Congenitos (www.fundacion1000.es), of Spain. We gratefully acknowledge the patient and his family for their excellent collaboration.

Repositorio Institucional de la Universidad de Oviedo

Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date

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