Para acceder a los documentos con el texto completo, por favor, siga el siguiente enlace: http://hdl.handle.net/2445/126149
dc.contributor.author | Eggermann, Thomas |
---|---|
dc.contributor.author | Netchine, Irène |
dc.contributor.author | Temple, I. Karen |
dc.contributor.author | Tümer, Zeynep |
dc.contributor.author | Monk, Dave Nicholas |
dc.contributor.author | Mackay, Deborah |
dc.contributor.author | Grønskov, Karin |
dc.contributor.author | Riccio, Andrea |
dc.contributor.author | Linglart, Agnès |
dc.contributor.author | Maher, Eamonn R. |
dc.date | 2018-11-15T15:33:05Z |
dc.date | 2018-11-15T15:33:05Z |
dc.date | 2015-03-14 |
dc.date | 2018-07-24T12:32:45Z |
dc.identifier.uri | http://hdl.handle.net/2445/126149 |
dc.format | 10 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | BioMed Central Ltd |
dc.relation | Reproducció del document publicat a: https://doi.org/10.1186/s13148-015-0050-z |
dc.relation | Clinical Epigenetics, 2015, vol. 7, num. 23 |
dc.relation | https://doi.org/10.1186/s13148-015-0050-z |
dc.rights | cc by (c) Eggermann et al., 2015 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.rights | http://creativecommons.org/licenses/by/3.0/es/ |
dc.subject | Malalties hereditàries |
dc.subject | Malalties rares |
dc.subject | Genetic diseases |
dc.subject | Rare diseases |
dc.title | Congenital imprinting disorders: EUCID.net - a network to decipher their aetiology and to improve the diagnostic and clinical care |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |