Browsing by Author Verma, Ankit
Showing results 1 to 2 of 2
| Issue Date | Title | Author(s) |
|---|---|---|
| 17-Dec-2019 | A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation | Demond, Hannah; Anvar, Zahra; Jahromi, Bahia Namavar; Sparago, Angela; Verma, Ankit; Davari, Maryam; Calzari, Luciano; Russo, Silvia; Jahromi, Mojgan Akbarzadeh; Monk, David; Andrews, Simon; Riccio, Andrea; Kelsey, Gavin |
| 28-May-2022 | 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 | Pignata, Laura; Cecere, Francesco; Verma, Ankit; Hay Mele, Bruno; Monticelli, Maria; Acurzio, Basilia; Giaccari, Carlo; Sparago, Angela; Hernandez Mora, Jose Ramon; Monteagudo Sánchez, Ana; Esteller, Manel; Pereda, Arrate; Tenorio Castano, Jair; Palumbo, Orazio; Carella, Massimo; Prontera, Paolo; Piscopo, Carmelo; Accadia, Maria; Lapunzina, Pablo; Cubellis, Maria Vittoria; Perez de Nanclares, Guiomar; Monk, David; Riccio, Andrea; Cerrato, Flavia |