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.
Revue:
Clinical Epigenetics

ISSN: 1868-7083,  1868-7075

Année de publication: 2024

Volumen: 16

Número: 1

Type: Article

DOI: 10.1186/S13148-024-01652-8 GOOGLE SCHOLAR lock_openAccès ouvert editor
La source de données: Scopus