Search

Author/Creator Cereda, A.

1. Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange‐overlapping phenotype. Issue 1 (25th February 2015)

Authors:
Parenti, I.; Gervasini, C.; Pozojevic, J.; Graul‐Neumann, L.; Azzollini, J.; Braunholz, D.; Watrin, E.; Wendt, K.S.; Cereda, A.; Cittaro, D.; Gillessen‐Kaesbach, G.; Lazarevic, D.; Mariani, M.; Russo, S.; Werner, R.; Krawitz, P.; Larizza, L.; Selicorni, A.; Kaiser, F.J.
Journal:
Clinical genetics
Issue:
Volume 89:Issue 1(2016)
Page Start:
74
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. Issue 9 (2nd September 2018)

Authors:
Fontana, L.; Bedeschi, M. F.; Maitz, S.; Cereda, A.; Faré, C.; Motta, S.; Seresini, A.; D'Ursi, P.; Orro, A.; Pecile, V.; Calvello, M.; Selicorni, A.; Lalatta, F.; Milani, D.; Sirchia, S. M.; Miozzo, M.; Tabano, S.
Journal:
Epigenetics
Issue:
Volume 13:Issue 9(2018)
Page Start:
897
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Expanding the clinical spectrum of the 'HDAC8‐phenotype' – implications for molecular diagnostics, counseling and risk prediction. Issue 5 (25th January 2016)

Authors:
Parenti, I.; Gervasini, C.; Pozojevic, J.; Wendt, K.S.; Watrin, E.; Azzollini, J.; Braunholz, D.; Buiting, K.; Cereda, A.; Engels, H.; Garavelli, L.; Glazar, R.; Graffmann, B.; Larizza, L.; Lüdecke, H.J.; Mariani, M.; Masciadri, M.; Pié, J.; Ramos, F.J.; Russo, S.
Journal:
Clinical genetics
Issue:
Volume 89:Issue 5(2016)
Page Start:
564
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗