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.
Revue:
Clinical Epigenetics

ISSN: 1868-7083,  1868-7075

Année de publication: 2022

Volumen: 14

Número: 1

Type: Article

DOI: 10.1186/S13148-022-01292-W GOOGLE SCHOLAR lock_openAccès ouvert editor

Objectifs de Développement Durable

La source de données: Scopus