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Your search keyword '"Venturi, Marina"' showing total 26 results
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26 results on '"Venturi, Marina"'

2. Validation of a large Italian database of 15 STR loci

Author

Presciuttini, Silvano, Cerri, Nicoletta, Turrina, Stefania, Pennato, Benedetto, Alu, Milena, Asmundo, Alessio, Barbaro, Anna, Boschi, Ilaria, Buscemi, Loredana, Caenazzo, Luciana, Carnevali, Eugenia, De Leo, Domenico, Di Nunno, Cosimo, Domenici, Ranieri, Maniscalco, Michela, Peloso, Gabriella, Pelotti, Susi, Piccinini, Andrea, Podini, Daniele, Ricci, Ugo, Robino, Carlo, Saravo, Luigi, Verzeletti, Andrea, Venturi, Marina, and Tagliabracci, Adriano

Subjects
Human population genetics -- Research -- Analysis, Allelomorphism -- Analysis -- Research, Health, Law
Abstract

Abstract Results from a collaborative exercise with proficiency testing conducted by 20 Italian laboratories on the 15 loci included in the Identifiler® kit were analyzed by allele sharing methods and [...]

Published
2006

26. A novel frameshift mutation (+A) at codon 18 of the beta-globin gene associated with high persistence of fetal hemoglobin phenotype and deltabeta-thalassemia.

Author

Feriotto G, Salvatori F, Finotti A, Breveglieri G, Venturi M, Zuccato C, Bianchi N, Borgatti M, Lampronti I, Mancini I, Massei F, Favre C, and Gambari R

Subjects
Cells, Cultured, Child, Chromatography, High Pressure Liquid, DNA genetics, Exons, Female, Gene Deletion, Gene Dosage, Humans, Immunohistochemistry, Molecular Sequence Data, Phenotype, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, DNA, Codon, Fetal Hemoglobin genetics, Frameshift Mutation, Globins genetics, Thalassemia genetics
Abstract

We report in this paper a novel thalassemia mutation (insertion of a single A nucleotide within the exon 1, at codon 18, of the beta-globin gene) associated with a deletion of the deltabeta-globin gene region, in a patient exhibiting high persistence of fetal hemoglobin. The novel mutation causes a frameshift with the generation of a UGA stop codon. Analysis of the parent's DNA demonstrates that the A insertion and frameshift mutation are inherited from the father, while the deltabeta-globin gene deletion is inherited from the mother. Gene dosage analysis and deletion-specific PCR demonstrate that the deletion is the (deltabeta)(0) Sicilian deletion, involving a 13.4-kb deltabeta-globin gene region., (2008 S. Karger AG, Basel)

Published
2008
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