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American Journal of Medical Genetics. Part A|June 9, 2005
Prenatal diagnosis of chromosome 4 mosaicism: prognostic role of cytogenetic, molecular, and ultrasound/MRI characterizationMattia Gentile, Paolo Volpe, Filomena Cariola, et al.
American Journal of Medical Genetics. Part A|March 22, 2021
First prenatal case of Noonan syndrome with SOS2 mutation: Implications of early diagnosis for genetic counselingMattia Gentile, Tiziana Fanelli, Francesca Romana Lepri, et al.
European Journal of Medical Genetics|June 10, 2006
Interstitial 1q43-q43 deletion with left ventricular noncompaction myocardiumNobuko Kanemoto, Hitoshi Horigome, Junko Nakayama, et al.
Diagnostics (Basel, Switzerland)|July 12, 2025
Brittle Cornea Syndrome: Molecular Diagnosis and ManagementMarco Zeppieri, Mattia Gentile, Antonio Acquaviva, et al.
American Journal of Medical Genetics. Part A|May 6, 2016
14q13 distal microdeletion encompassing NKX2-1 and PAX9: Patient report and refinement of the associated phenotypeMattia Gentile, Delia De Mattia, Angela Pansini, et al.
Cancer Biomarkers : Section a of Disease Markers|April 26, 2018
Clinical biomarkers for cancer recognition and prevention: A novel approach with optical measurementsGiuseppe Latini, Claudio De Felice, Alessandro Barducci, et al.
Pathology International|June 4, 2009
Characterization of a complex chromosome aberration in two cases of peritoneal mesothelioma arising primarily in the hernial sacGabriella Serio, Mattia Gentile, Antonio Pennella, et al.
International Journal of Medical Sciences|November 10, 2010
Non-syndromic multiple supernumerary teeth in a family unit with a normal karyotype: case reportFrancesco Inchingolo, Marco Tatullo, Fabio M Abenavoli, et al.
Human Reproduction (Oxford, England)|February 25, 2006
Chromosomal rearrangements in Xq and premature ovarian failure: mapping of 25 new cases and review of the literatureFlavio Rizzolio, Silvia Bione, Cinzia Sala, et al.
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