Novel 14q32.2 paternal deletion encompassing the whole DLK1 gene associated with Temple syndrome

  1. Baena, N.
  2. Monk, D.
  3. Aguilera, C.
  4. Fraga, M.F.
  5. Fernández, A.F.
  6. Gabau, E.
  7. Corripio, R.
  8. Capdevila, N.
  9. Trujillo, J.P.
  10. Ruiz, A.
  11. Guitart, M.
Journal:
Clinical Epigenetics

ISSN: 1868-7083 1868-7075

Year of publication: 2024

Volume: 16

Issue: 1

Type: Article

DOI: 10.1186/S13148-024-01652-8 GOOGLE SCHOLAR lock_openOpen access editor