Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date
American Journal of Medical Genetics, Part A, 167(9), p. 2034-2041 (2015); doi:10.1002/ajmg.a.37117
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.
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