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Molecular and Clinical Analyses of Greig Cephalopolysyndactyly and Pallister-Hall Syndromes: Robust Phenotype Prediction from the Type and Position of GLI3 Mutations

Mendelian DisorderGenetic DisorderMedicineGeneticsGenetic EpidemiologyPathologyGli3 MutationsDisease Gene IdentificationMolecular MedicinePallister-hall SyndromesRobust Phenotype PredictionVariant InterpretationClinical Genetics