HuGE Literature Finder
Records
1
-
5
| Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups. American journal of medical genetics. Part A 2016 Jul . Maas Saskia M, Vansenne Fleur, Kadouch Daniel J M, Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M, Merks Johannes H M, Maher Eamonn R, Hennekam Raoul |
| Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol. The Journal of pediatrics 2016 Jun . Mussa Alessandro, Molinatto Cristina, Baldassarre Giuseppina, Riberi Evelise, Russo Silvia, Larizza Lidia, Riccio Andrea, Ferrero Giovanni Battis |
| Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance. Hormone research in pædiatrics 2013 80 (6): 457-65. Brioude F, Lacoste A, Netchine I, Vazquez M-P, Auber F, Audry G, Gauthier-Villars M, Brugieres L, Gicquel C, Le Bouc Y, Rossignol |
| Studies of variations of the cyclin-dependent kinase inhibitor 1C and the cyclin-dependent kinase 4 genes in relation to type 2 diabetes mellitus and related quantitative traits. Journal of molecular medicine (Berlin, Germany) 2005 May 83 (5): 353-61. Nielsen Eva-Maria D, Hansen Lars, Stissing Trine, Yanagisawa Keiko, Borch-Johnsen Knut, Poulsen Pernille, Vaag Allan, Hansen Torben, Pedersen Ol |
| An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype. Human molecular genetics 2004 Jan 13 (2): 247-55. Murrell Adele, Heeson Sarah, Cooper Wendy N, Douglas Eleanor, Apostolidou Sophia, Moore Gudrun E, Maher Eamonn R, Reik Wo |
- Page last reviewed:Oct 1, 2021
- Page last updated:Jun 28, 2022
- Content source: