{
    "PMID": "10424811",
    "TI": "Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.",
    "JT": "Journal of medical genetics",
    "BTI": "",
    "DP": "1999-07",
    "AU": "Lam W W, Hatada I, Ohishi S, Mukai T, Joyce J A, Cole T R, Donnai D, Reik W, Schofield P N, Maher E R"
}