Associated Papers
Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder.
Brunet T et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2021
33173220 (PubMed )
Supplement: 41436_2020_993_MOESM1_ESM.pdf
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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