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

Author:
Martínez-Fernández, María Luisa; Fernández Toral, JoaquínUniovi authority; Llano Rivas, IsabelUniovi authority; Bermejo-Sánchez, Eva; MacDonald, Alexandra; Martínez-Frías, María Luisa
Publication date:
2015
Publisher version:
http://dx.doi.org/10.1002/ajmg.a.37117
Citación:
American Journal of Medical Genetics, Part A, 167(9), p. 2034-2041 (2015); doi:10.1002/ajmg.a.37117
Descripción física:
p. 2034-2041
URI:
http://hdl.handle.net/10651/34157
ISSN:
1552-4825
DOI:
10.1002/ajmg.a.37117
Patrocinado por:

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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