Anna Ravani
Ferrara, Italy
Last Updated: 09/26/2026
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Found 12 publications
Can paranasal sinus computed tomography screen for cystic fibrosis heterozygotes?
Journal: Panminerva medica
Published: February 13, 2019
Workload measurement for molecular genetics laboratory: A survey study.
Journal: PloS one
Published: May 11, 2018
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript.
Journal: Neuromuscular disorders : NMD
Published: November 23, 2015
A rare case of Hemoglobin Leiden interfering with the DIFF channel of Sysmex XE-2100.
Journal: Scandinavian journal of clinical and laboratory investigation
Published: April 16, 2015
New and rare GJB2 alleles in patients with nonsyndromic sensorineural hearing impairment: a genotype/auditory phenotype correlation.
Journal: Genetic testing and molecular biomarkers
Published: November 18, 2014
Genetic counseling for women referred for advanced maternal age: a telegenetic approach.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: October 08, 2014
Characterization of Hb Calvino (HBB: c.406G > A): a new silent β-globin gene variant found in coexistence with α-thalassemia in a family of African origin.
Journal: Hemoglobin
Published: September 16, 2014
The high oxygen affinity haemoglobin Nantes: a family case description.
Journal: Blood transfusion = Trasfusione del sangue
Published: August 17, 2014
Novel mutations in the SLC26A4 gene.
Journal: International journal of pediatric otorhinolaryngology
Published: February 23, 2012
Universal neonatal screening for sickle cell disease and other haemoglobinopathies in Ferrara, Italy.
Journal: Blood transfusion = Trasfusione del sangue
Published: February 21, 2012
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Last Updated: 09/26/2026