Novel 14q32.2 paternal deletion encompassing the whole dlk1 gene associated with temple syndrome
| dc.contributor.author | Baena, N. | |
| dc.contributor.author | Monk, D. | |
| dc.contributor.author | Aguilera, C. | |
| dc.contributor.author | Fernández Fraga, Mario | |
| dc.contributor.author | Fernández Fernández, Agustín | |
| dc.contributor.author | Gabau, E. | |
| dc.contributor.author | Corripio, R. | |
| dc.contributor.author | Capdevila, N. | |
| dc.contributor.author | Trujillo, J. P. | |
| dc.contributor.author | Ruiz A. | |
| dc.contributor.author | Guitart, M. | |
| dc.date.accessioned | 2024-10-22T06:07:55Z | |
| dc.date.available | 2024-10-22T06:07:55Z | |
| dc.date.issued | 2024 | |
| dc.identifier.citation | Clinical Epigenetics, 16(1), (2024); doi:10.1186/s13148-024-01652-8 | |
| dc.identifier.issn | 1868-7075 | |
| dc.identifier.uri | https://hdl.handle.net/10651/75265 | |
| dc.language.iso | eng | |
| dc.relation.ispartof | Clinical Epigenetics | |
| dc.rights | © The Author(s) 2024 | |
| dc.rights | CC Reconocimiento Universal | |
| dc.rights.uri | http://creativecommons.org/publicdomain/zero/1.0/ | |
| dc.source | Scopus | |
| dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85192221500&doi=10.1186%2fs13148-024-01652-8&partnerID=40&md5=3585dc8baff8566b98c12d21ebdca3f2 | |
| dc.title | Novel 14q32.2 paternal deletion encompassing the whole dlk1 gene associated with temple syndrome | |
| dc.type | journal article | |
| dc.identifier.doi | 10.1186/s13148-024-01652-8 | |
| dc.relation.publisherversion | http://dx.doi.org/10.1186/s13148-024-01652-8 | |
| dc.rights.accessRights | open access | |
| dc.type.hasVersion | VoR |
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