| Bibliographic Citation
| - Brioude Frederic, Netchine Irène, Praz Françoise, Le Jule Marilyne, Calmel Claire, Lacombe Didier, Edery Patrick, Catala Martin, Odent Sylvie, Isidor Bertrand, Lyonnet Stanislas, Sigaudy Sabine, Leheup Bruno, Audebert-Bellanger Séverine, Burglen Lydie, Giuliano Fabienne, Alessandri Jean-Luc, Cormier-Daire Valérie, Laffargue Fanny, Blesson Sophie, Coupier Isabelle, Lespinasse James, Blanchet Patricia, Boute Odile, Baumann Clarisse, Polak Michel, Doray Bérénice, Verloes Alain, Viot Géraldine, Le Bouc Yves, Rossignol Sylvie. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization. Human Mutation, Wiley, 2015, 36 (9), pp.894--902. ⟨10.1002/humu.22824⟩
- Brioude Frederic, Netchine Irène, Praz Françoise, Le Jule Marilyne, Calmel Claire, Lacombe Didier, Edery Patrick, Catala Martin, Odent Sylvie, Isidor Bertrand, Lyonnet Stanislas, Sigaudy Sabine, Leheup Bruno, Audebert-Bellanger Séverine, Burglen Lydie, Giuliano Fabienne, Cormier-Daire Valérie, Laffargue Fanny, Coupier Isabelle, Lespinasse James, Blanchet Patricia, Boute Odile, Baumann Clarisse, Polak Michel, Doray Bérénice, Verloes Alain, Viot Géraldine, Rossignol Sylvie. Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization. Human Mutation, Wiley, 2015, 36 (9), pp.894--902. ⟨10.1002/humu.22824⟩
- Brioude Frederic, Netchine Irène, Praz Françoise, Le Jule Marilyne, Calmel Claire, Lacombe Didier, Edery Patrick, Catala Martin, Odent Sylvie, Isidor Bertrand, Lyonnet Stanislas, Sigaudy Sabine, Leheup Bruno, Audebert-Bellanger Séverine, Burglen Lydie, Giuliano Fabienne, Cormier-Daire Valérie, Laffargue Fanny, Coupier Isabelle, Lespinasse James, Blanchet Patricia, Boute Odile, Baumann Clarisse, Polak Michel, Doray Bérénice, Verloes Alain, Viot Géraldine, Rossignol Sylvie . Mutations of the Imprinted CDKN1C Gene as a Cause of the Overgrowth Beckwith–Wiedemann Syndrome: Clinical Spectrum and Functional Characterization . Human Mutation, 2015, 36 (9), pp.894--902 . ⟨10.1002/humu.22824⟩
|
![[RDF Data]](/fct/images/sw-rdf-blue.png)
