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Chiara Pescucci

Showing results (1-10 of 29) with videos related to

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Nature Genetics|December 30, 2004
Is Rett syndrome a loss-of-imprinting disorder?Chiara Pescucci, Ilaria Meloni, Alessandra Renieri
Journal of Nephrology|May 28, 2003
Type-IV collagen related diseasesChiara Pescucci, Ilaria Longo, Mirella Bruttini, et al.
Bioinformatics (Oxford, England)|October 25, 2012
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScriptMatteo Benelli, Chiara Pescucci, Giuseppina Marseglia, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 17, 2003
Rett syndrome: the complex nature of a monogenic diseaseAlessandra Renieri, Ilaria Meloni, Ilaria Longo, et al.
Cancer Genetics and Cytogenetics|December 14, 2004
Chromosomal alterations detected by comparative genomic hybridization in nonfunctioning endocrine pancreatic tumorsGiovanna Floridia, Giulia Grilli, Marco Salvatore, et al.
American Journal of Medical Genetics. Part A|March 14, 2007
Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGHMaria Antonietta Mencarelli, Rossella Caselli, Chiara Pescucci, et al.
International Journal of Fertility & Sterility|March 18, 2016
Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The LiteratureAlfredo Orrico, Giuseppina Marseglia, Chiara Pescucci, et al.
Clinical Dysmorphology|April 20, 2013
An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformationAmbra Cortesi, Maja Rossi, Marta Mazzi, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 28, 2006
Optineurin gene is not involved in the common high-tension form of primary open-angle glaucomaFrancesca Ariani, Ilaria Longo, Paolo Frezzotti, et al.
European Journal of Medical Genetics|December 3, 2014
16p11.2 de novo microdeletion encompassing SRCAP gene in a patient with speech impairment, global developmental delay and behavioural problemsFrancesca Gerundino, Guiseppina Marseglia, Chiara Pescucci, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Nature Genetics|December 30, 2004
Is Rett syndrome a loss-of-imprinting disorder?Chiara Pescucci, Ilaria Meloni, Alessandra Renieri
Journal of Nephrology|May 28, 2003
Type-IV collagen related diseasesChiara Pescucci, Ilaria Longo, Mirella Bruttini, et al.
Bioinformatics (Oxford, England)|October 25, 2012
Discovering chimeric transcripts in paired-end RNA-seq data by using EricScriptMatteo Benelli, Chiara Pescucci, Giuseppina Marseglia, et al.
Journal of Molecular Medicine (Berlin, Germany)|May 17, 2003
Rett syndrome: the complex nature of a monogenic diseaseAlessandra Renieri, Ilaria Meloni, Ilaria Longo, et al.
Cancer Genetics and Cytogenetics|December 14, 2004
Chromosomal alterations detected by comparative genomic hybridization in nonfunctioning endocrine pancreatic tumorsGiovanna Floridia, Giulia Grilli, Marco Salvatore, et al.
American Journal of Medical Genetics. Part A|March 14, 2007
Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGHMaria Antonietta Mencarelli, Rossella Caselli, Chiara Pescucci, et al.
International Journal of Fertility & Sterility|March 18, 2016
Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The LiteratureAlfredo Orrico, Giuseppina Marseglia, Chiara Pescucci, et al.
Clinical Dysmorphology|April 20, 2013
An additional case of cerebrofaciothoracic dysplasia associated with Chiari type I malformationAmbra Cortesi, Maja Rossi, Marta Mazzi, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 28, 2006
Optineurin gene is not involved in the common high-tension form of primary open-angle glaucomaFrancesca Ariani, Ilaria Longo, Paolo Frezzotti, et al.
European Journal of Medical Genetics|December 3, 2014
16p11.2 de novo microdeletion encompassing SRCAP gene in a patient with speech impairment, global developmental delay and behavioural problemsFrancesca Gerundino, Guiseppina Marseglia, Chiara Pescucci, et al.
Pageof 3