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.
Journal:
Clinical Epigenetics

ISSN: 1868-7083,  1868-7075

Year of publication: 2022

Volume: 14

Issue: 1

Type: Article

DOI: 10.1186/S13148-022-01292-W GOOGLE SCHOLAR lock_openOpen access editor

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Data source: Scopus