Associated Papers
Familial Beckwith-Wiedemann syndrome in a multigenerational family: Forty years of careful phenotyping.
Best LG et al.
American Journal of Medical Genetics. Part A, 2023
Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants.
Cardoso LCA et al.
Cancers, 2022
Increased protein stability of CDKN1C causes a gain-of-function phenotype in patients with IMAGe syndrome.
Hamajima N et al.
Plos One, 2013
Mutations in the PCNA-binding domain of CDKN1C cause IMAGe syndrome.
Arboleda VA et al.
Nature Genetics, 2012
CDKN1C (p57(Kip2)) analysis in Beckwith-Wiedemann syndrome (BWS) patients: Genotype-phenotype correlations, novel mutations, and polymorphisms.
Romanelli V et al.
American Journal of Medical Genetics. Part A, 2010
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