Maria Roberta Tremolaterra

Analysis of Dystrophin Gene Deletions Indicates that the Hinge III Region of the Protein Correlates with Disease Severity

Antonella Carsana, Giulia Frisso, Maria Roberta Tremolaterra et al. · Annals of Human Genetics · 2005 · 46 citations

Genetics, Becker Muscular Dystrophy, Pathology +17

Analysis of Dystrophin Gene Deletions Indicates that the Hinge III Region of the Protein Correlates with Disease Severity

Antonella Carsana, Giulia Frisso, Maria Roberta Tremolaterra et al. · Annals of Human Genetics · 2005 · 46 citations

Genetics, Genetic Epidemiology, Becker Muscular Dystrophy +27

A Larger Spectrum of Intragenic Short Tandem Repeats Improves Linkage Analysis and Localization of Intragenic Recombination Detection in the Dystrophin Gene

Antonella Carsana, Giulia Frisso, Maria Roberta Tremolaterra et al. · Journal of Molecular Diagnostics · 2007 · 20 citations · Full text

Dystrophin Gene, Mendelian Disorder, Genetic Disorder +9

Prenatal molecular diagnosis of inherited neuromuscular diseases: Duchenne/Becker muscular dystrophy, myotonic dystrophy type 1 and spinal muscular atrophy

Gabriella Esposito, Raffaella Ruggiero, Maria Flavia Savarese et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2013 · 18 citations

Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD gene

Gabriella Esposito, Maria Roberta Tremolaterra, Evelina Marsocci et al. · Journal of Human Genetics · 2017 · 18 citations

Deletion Breakpoints, Dmd Gene, Genetics +9