| 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 | |
