Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances

  1. Pignata, L.
  2. Cecere, F.
  3. Verma, A.
  4. Hay Mele, B.
  5. Monticelli, M.
  6. Acurzio, B.
  7. Giaccari, C.
  8. Sparago, A.
  9. Hernandez Mora, J.R.
  10. Monteagudo-Sánchez, A.
  11. Esteller, M.
  12. Pereda, A.
  13. Tenorio-Castano, J.
  14. Palumbo, O.
  15. Carella, M.
  16. Prontera, P.
  17. Piscopo, C.
  18. Accadia, M.
  19. Lapunzina, P.
  20. Cubellis, M.V.
  21. de Nanclares, G.P.
  22. Monk, D.
  23. Riccio, A.
  24. Cerrato, F.
Aldizkaria:
Clinical Epigenetics

ISSN: 1868-7083,  1868-7075

Argitalpen urtea: 2022

Alea: 14

Zenbakia: 1

Mota: Artikulua

DOI: 10.1186/S13148-022-01292-W GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus