Marcello Morgutti
Trieste, Italy
Last Updated: 09/26/2026
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Found 8 publications
Things come in threes: A new complex allele and a novel deletion within the CFTR gene complicate an accurate diagnosis of cystic fibrosis.
Journal: Molecular genetics & genomic medicine
Published: June 07, 2021
Next generation sequencing study in a cohort of Italian patients with syndromic hearing loss.
Journal: Hearing research
Published: April 11, 2019
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number Variations.
Journal: Frontiers in genetics
Published: May 03, 2018
Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients.
Journal: Genetics and molecular research : GMR
Published: December 16, 2014
Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis.
Journal: Hearing research
Published: August 30, 2014
A real-time polymerase chain reaction-based protocol for low/medium-throughput Y-chromosome microdeletions analysis.
Journal: Genetic testing and molecular biomarkers
Published: October 30, 2012
CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients.
Journal: Genes and immunity
Published: June 01, 2012
Showing 1-8 of 8
Last Updated: 09/26/2026