Sfoglia per RIVISTA
EUROPEAN JOURNAL OF HUMAN GENETICS : EJHG
Collezione AOU San Luigi di Orbassano

  

Items : 2

Identification of the DNA methylation signature of Mowat-Wilson syndrome. in European journal of human genetics : EJHG / Eur J Hum Genet. 2024 Jun;32(6):619-629. doi: 10.1038/s41431-024-01548-4. Epub 2024 Feb 13.

2024
AOU Città della Salute di Torino
AOU San Luigi di Orbassano

Garavelli L; Sadikovic B; Tartaglia M; Ferrero GB; McConkey H; Pullano V; Zollino M; Pavinato L; Sukarova E; Brusco A; Baldo C; Mandrile G; Lauzon C; Cordelli DM; Ivanovski I; Fetta A; Haghshenas S; Levy MA; Relator R; Zuntini R; Caraffi SG; van der Laan L; Rooney K; Trajkova S;

Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes. in European journal of human genetics : EJHG / Eur J Hum Genet. 2023 Nov;31(11):1228-1236. doi: 10.1038/s41431-023-01324-w. Epub 2023 Mar 6.

2023
AOU Città della Salute di Torino
AOU San Luigi di Orbassano

Pasini B; De Rubeis S; Buxbaum JD; Ferrero GB; Brusco A; Delledonne M; Pippucci T; Tartaglia M; Rossato M; Mandrile G; Froukh T; Bruselles A; Dimartino P; Mussa A; Carli D; Palermo F; Fadda A; Bertoli L; Pavinato L; Cardaropoli S; Pullano V; Ferrero E; Sukarova-Angelovska E; Carestiato S; Trajkova S; Battaglia A; Rinninella A; Salmin P; Giovenino C; et alii...