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

dc.contributor.author	Martínez-Fernández, María Luisa
dc.contributor.author	Fernández Toral, Joaquín
dc.contributor.author	Llano Rivas, Isabel
dc.contributor.author	Bermejo-Sánchez, Eva
dc.contributor.author	MacDonald, Alexandra
dc.contributor.author	Martínez-Frías, María Luisa
dc.date.accessioned	2015-12-21T10:40:00Z
dc.date.available	2015-12-21T10:40:00Z
dc.date.issued	2015
dc.identifier.citation	American Journal of Medical Genetics, Part A, 167(9), p. 2034-2041 (2015); doi:10.1002/ajmg.a.37117
dc.identifier.issn	1552-4825
dc.identifier.uri	http://hdl.handle.net/10651/34157
dc.description.sponsorship	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.
dc.format.extent	p. 2034-2041
dc.language.iso	eng
dc.relation.ispartof	American Journal of Medical Genetics, Part A
dc.rights	© 2015 Wiley Periodicals, Inc.
dc.source	Scopus
dc.source.uri	http://www.scopus.com/inward/record.url?eid=2-s2.0-84939472882&partnerID=40&md5=667559abb8923b03facaabb25493a300
dc.title	Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date
dc.type	journal article
dc.identifier.doi	10.1002/ajmg.a.37117
dc.relation.publisherversion	http://dx.doi.org/10.1002/ajmg.a.37117

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