Browsing by Author Russo, Silvia
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 |
| 1-Jan-2018 | Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains | Monk, David; Morales, Joannella; den Dunnen, Johan T.; Russo, Silvia; Court, Franck; Prawitt, Dirk; Eggermann, Thomas; Beygo, Jasmin; Buiting, Karin; Tumer, Zeynep; Nomenclature group of the European Network for Human Congenital Imprinting Disorders |