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.
Aldizkaria:
Clinical Epigenetics

ISSN: 1868-7083,  1868-7075

Argitalpen urtea: 2024

Alea: 16

Zenbakia: 1

Mota: Artikulua

DOI: 10.1186/S13148-024-01652-8 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus