<style face="normal" font="default" size="100%">Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis.</style>

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<style face="normal" font="default" size="100%">Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis.</style>

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<style face="normal" font="default" size="100%">Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients.</style>

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<style face="normal" font="default" size="100%">CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients.</style>

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<style face="normal" font="default" size="100%">Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North-Eastern Italy.</style>