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Amplification failure of the amelogenin gene ( AMELX ) caused by a primer binding site mutation

2009; Wiley; Volume: 29; Issue: 12 Linguagem: Inglês

10.1002/pd.2389

1097-0223

Stefano Caratti, Gianfranco Voglino, Vincenzo Cirigliano, A. Ghidini, Riccardo Taulli, Carlo Torre, Carlo Robino,

Renal and related cancers

Prenatal DiagnosisVolume 29, Issue 12 p. 1180-1182 Research Letter Amplification failure of the amelogenin gene (AMELX) caused by a primer binding site mutation S. Caratti, S. Caratti Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, ItalySearch for more papers by this authorG. Voglino, G. Voglino Molecular Genetics and Cytogenetics Laboratory, Promea S.P.A., Turin, ItalySearch for more papers by this authorV. Cirigliano, V. Cirigliano Departamento de Genètica Molecular, General Laboratory, Barcelona, Spain Departament de Biologia Cellular, Fisiologia, Universitat Autònoma de Barcelona, Bellaterra, SpainSearch for more papers by this authorA. Ghidini, A. Ghidini Department of Obstetrics and Gynaecology, Prenatal Diagnosis Service, Borgo Trento Hospital, Verona, ItalySearch for more papers by this authorR. Taulli, R. Taulli Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, Italy Centre for Experimental Research and Medical Studies (CeRMS), University of Turin, Turin, ItalySearch for more papers by this authorC. Torre, C. Torre Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, ItalySearch for more papers by this authorCarlo Robino, Corresponding Author Carlo Robino [email protected] Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, ItalyDepartment of Anatomy, Pharmacology and Legal Medicine, University of Turin, Corso Galileo Galilei 22, 10126 Turin, Italy.Search for more papers by this author S. Caratti, S. Caratti Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, ItalySearch for more papers by this authorG. Voglino, G. Voglino Molecular Genetics and Cytogenetics Laboratory, Promea S.P.A., Turin, ItalySearch for more papers by this authorV. Cirigliano, V. Cirigliano Departamento de Genètica Molecular, General Laboratory, Barcelona, Spain Departament de Biologia Cellular, Fisiologia, Universitat Autònoma de Barcelona, Bellaterra, SpainSearch for more papers by this authorA. Ghidini, A. Ghidini Department of Obstetrics and Gynaecology, Prenatal Diagnosis Service, Borgo Trento Hospital, Verona, ItalySearch for more papers by this authorR. Taulli, R. Taulli Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, Italy Centre for Experimental Research and Medical Studies (CeRMS), University of Turin, Turin, ItalySearch for more papers by this authorC. Torre, C. Torre Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, ItalySearch for more papers by this authorCarlo Robino, Corresponding Author Carlo Robino [email protected] Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, ItalyDepartment of Anatomy, Pharmacology and Legal Medicine, University of Turin, Corso Galileo Galilei 22, 10126 Turin, Italy.Search for more papers by this author First published: 19 October 2009 https://doi.org/10.1002/pd.2389Citations: 13AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. REFERENCES Alves C, Coelho M, Rocha J, Amorim A. 2006. The Amelogenin locus displays a high frequency of X homologue failures in Sao Tome Island (West Africa). In Progress in Forensic Genetics 11, A Amorim, F Corte-Real, N Morling (eds). Elsevier Science: Amsterdam; 271– 273. Cirigliano V, Sherlock J, Conway G, et al. 1999. Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCR. Prenat Diagn 19: 1099– 1103. Cirigliano V, Lewin P, Szpiro-Tapies S, et al. 2001. Assessment of new markers for the rapid detection of aneuploidies by quantitative fluorescent PCR (QF-PCR). Ann Hum Genet 65: 421– 427. Cirigliano V, Voglino G, Ordoñez E, et al. 2009. Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience. Prenat Diagn 29: 40– 49. Follenzi A, Ailles LE, Bakovic S, et al. 2000. 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Biotechniques 15: 636– 641. Citing Literature Volume29, Issue12December 2009Pages 1180-1182 ReferencesRelatedInformation