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Publications by G Antinolo
Genotype-Phenotype Relationship in 12 Patients Carrying Cystic Fibrosis Mutation R334W.
Journal of Medical Genetics
Genetics
Contribution of RET, NTRK3 and EDN3 to the Expression of Hirschsprung Disease in a Multiplex Family
Journal of Medical Genetics
Genetics
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Genotype–phenotype Association in Patients With SCN4A Mutation – Authors' Reply
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Genotype/Phenotype Association in Cystic Fibrosis: Analyses of the ΔF508, R553X, and 3905insT Mutations
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Genotype-Phenotype Relationship and Risk Stratification in Loss-Of-Function SCN5A Mutation Carriers
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Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation
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Phenotypic Expression of the p.Leu1077Pro CFTR Mutation in Sicilian Cystic Fibrosis Patients
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The Cystic Fibrosis F508del Mutation in Crohn's Disease
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Genotype-Specific Small-Molecule Therapy for Cystic Fibrosis
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