Published in
Elsevier, Journal of Pediatrics, (176), p. 142-149.e1
DOI: 10.1016/j.jpeds.2016.05.038
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Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol.
Journal article published in 2016 by
Alessandro Mussa 
,
Cristina Molinatto,
Giuseppina Baldassarre,
Evelise Riberi,
Silvia Russo ,
Lidia Larizza,
Andrea Riccio,
Giovanni Battista Ferrero
,
Cristina Molinatto,
Giuseppina Baldassarre,
Evelise Riberi,
Silvia Russo ,
Lidia Larizza,
Andrea Riccio,
Giovanni Battista Ferrero
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
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Abstract
To compare tumor risk in the 4 Beckwith-Wiedemann syndrome (BWS) molecular subgroups: Imprinting Control Region 1 Gain of Methylation (ICR1-GoM), Imprinting Control Region 2 Loss of Methylation (ICR2-LoM), Chromosome 11p15 Paternal Uniparental Disomy (UPD), and Cyclin-Dependent Kinase Inhibitor 1C gene (CDKN1C) mutation.