Publications by authors named "Maria Marinelli"

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Renal Hypoplasia and Oligomeganephronia in a Fetus with Wolf-Hirschhorn Syndrome.
Maria Paola Bonasoni, Mariangela Pati, Khush Shah, Andrea Musarò, Immacolata Blasi, Maria Marinelli

Diagnostics (Basel)· October 2025

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Prenatal Array-CGH Detection of 3q26.32q26.33 Interstitial Deletion Encompassing the Gene: Ultrasound, Pathological, and Cytogenetic Findings.
Maria Paola Bonasoni, Giuseppina Comitini, Mariangela Pati, Veronica Bizzarri, Veronica Barbieri, Maria Marinelli

Fetal Pediatr Pathol· December 2023

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Case Report: Sequential postzygotic mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving in oncogenic transformation.
Roberta Zuntini, Chiara Cattani, Lucia Pedace, Evelina Miele, Stefano Giuseppe Caraffi, Maria Marinelli

Front Genet· August 2023

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Prenatal Diagnosis of Fetal Trisomy 5 Mosaicism with Congenital Pulmonary Airway Malformation Type 3: A Case Report.
Maria Paola Bonasoni, Giuseppina Comitini, Gabriele Tonni, Silvia Asioli, Veronica Barbieri, Maria Marinelli

Fetal Pediatr Pathol· June 2022

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Mosaic Trisomy 12: Prenatal Diagnosis at Amniocentesis and Molecular Genetic Analysis on Fetal Tissues.
Paola Bonasoni, Gabriele Tonni, Giuseppina Comitini, Veronica Barbieri, Monia Rinaldini, Maria Marinelli

Fetal Pediatr Pathol· April 2022

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Clinical and Genetic Findings in a Series of Eight Families with Arthrogryposis.
Marzia Pollazzon, Stefano Giuseppe Caraffi, Silvia Faccioli, Simonetta Rosato, Heidi Fodstad, Maria Marinelli

Genes (Basel)· December 2021

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Whole Exome Sequencing Is the Minimal Technological Approach in Probands Born to Consanguineous Couples.
Francesca Peluso, Stefano Giuseppe Caraffi, Roberta Zuntini, Gabriele Trimarchi, Ivan Ivanovski, Maria Marinelli

Genes (Basel)· June 2021

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Landscape service flow dynamics in the metropolitan area of Córdoba (Argentina).
Maria Victoria Marinelli, Donatella Valente, Carlos Marcelo Scavuzzo, Irene Petrosillo

J Environ Manage· February 2021

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Expanding the phenotype of Wiedemann-Steiner syndrome: Craniovertebral junction anomalies.
Sara Giangiobbe, Stefano Giuseppe Caraffi, Ivan Ivanovski, Ilenia Maini, Marzia Pollazzon, Maria Marinelli

Am J Med Genet A· December 2020

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Workload measurement for molecular genetics laboratory: A survey study.
Enrico Tagliafico, Isabella Bernardis, Marina Grasso, Maria Rosaria D'Apice, Cristina Lapucci, Maria Marinelli

PLoS One· April 2019

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Endocrinological Abnormalities Are a Main Feature of 17p13.1 Microduplication Syndrome: A New Case and Literature Review.
Ilenia Maini, Ivan Ivanovski, Alessandro Iodice, Simonetta Rosato, Marzia Pollazzon, Maria Marinelli

Mol Syndromol· November 2016

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Unexpected results in the constitution of small supernumerary marker chromosomes.
Annalisa Vetro, Emmanouil Manolakos, Michael B Petersen, Loretta Thomaidis, Thomas Liehr, Maria Marinelli

Eur J Med Genet· March 2012

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Early detection (9+6 weeks) of cardiac failure in a fetus diagnosed as Turner syndrome by 2D transvaginal ultrasound-guided coelocentesis.
Gabriele Tonni, Daniela Azzoni, Alessandro Ventura, Claudio De Felice, Maria Marinelli

J Clin Ultrasound· June 2009

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Reversible immobilization of asiatic black bear (Ursus thibetanus) with detomidine-tiletamine-zolazepam and atipamezole.
Pietro Laricchiuta, Donatella Gelli, Marco Campolo, Maria Pia Marinelli, Olimpia R Lai

J Zoo Wildl Med· December 2008

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