Clinical characteristics and registry-validated extended pedigrees of germline TP53 mutation carriers in Denmark.

INTRODUCTION:TP53 mutation copyright (Li-Fraumeni Syndrome, LFS) cohort studies often suffer from lack of extensive pedigree exploration.METHODS:We performed a nation-wide exploration of TP53 mutation copyright families identified through all clinical genetics departments in Denmark.Pedigrees were expanded and verified using unique national person

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