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Publications by Alessandra Zanetti

A Hunter Patient With a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS Locus

Internal Medicine

Molecular Biology

English

Molecular Analysis of Turkish Maroteaux-Lamy Patients and Identification of One Novel Mutation in the Arylsulfatase B (ARSB) Gene

Internal Medicine

Molecular Biology

English

Related publications

Opposite Deletions/Duplications of the X Chromosome: Two Novel Reciprocal Rearrangements

European Journal of Human Genetics

English

Two Successful Natural Pregnancies in a Patient With Severe Uterine Prolapse: A Case Report

Journal of Medical Case Reports

English

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report

Frontiers in Genetics

Molecular Medicine

English

High-Throughput Sequencing of a 4.1 Mb Linkage Interval Reveals FLVCR2 Deletions and Mutations in Lethal Cerebral Vasculopathy

English

Fleece Variation in Alpaca (Vicugna Pacos): A Two-Locus Model for the Suri/Huacaya Phenotype

English

A DYW-protein Knockout inPhyscomitrellaaffects Two Closely Spaced Mitochondrial Editing Sites and Causes a Severe Developmental Phenotype

English

Genome-Wide Association Reveals Three SNPs Associated With Sporadic Amyotrophic Lateral Sclerosis Through a Two-Locus Analysis

BMC Medical Genetics

English

Interleukin-1 Two-Locus Haplotype Is Strongly Associated With Severe Chronic Periodontitis Among Yemenis

Molecular Biology International

English

Genotype and Phenotype Analyses in 136 Patients With Single Large-Scale Mitochondrial DNA Deletions

Journal of Human Genetics

English