Bilaketaren emaitzak - Francesca Romana Grati

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  1. 1
    Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis

    Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis nork Francesca Romana Grati

    Argitaratua 2014
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  2. 2
    Implications of fetoplacental mosaicism on cell‐free <scp>DNA</scp> testing: a review of a common biological phenomenon

    Implications of fetoplacental mosaicism on cell‐free <scp>DNA</scp> testing: a review of a common biological phenomenon nork Francesca Romana Grati

    Argitaratua 2016
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  3. 3
    Genome‐wide non‐invasive prenatal screening for all cytogenetically visible imbalances

    Genome‐wide non‐invasive prenatal screening for all cytogenetically visible imbalances nork Peter Benn, Francesca Romana Grati

    Argitaratua 2018
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    Editorial
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  4. 4
    Chromosomal mosaicism: Origins and clinical implications in preimplantation and prenatal diagnosis

    Chromosomal mosaicism: Origins and clinical implications in preimplantation and prenatal diagnosis nork Brynn Levy, Eva R. Hoffmann, Rajiv C. McCoy, Francesca Romana Grati

    Argitaratua 2021
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  5. 5
    An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening

    An evidence-based scoring system for prioritizing mosaic aneuploid embryos following preimplantation genetic screening nork Francesca Romana Grati, Gloria Gallazzi, Lara Branca, Federico Maggi, Giuseppe Simoni, Yuval Yaron

    Argitaratua 2018
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  6. 6
    Misbehaviour of XIST RNA in Breast Cancer Cells

    Misbehaviour of XIST RNA in Breast Cancer Cells nork Silvia Maria Sirchia, Silvia Tabano, Laura Monti, Maria Paola Recalcati, Manuela Gariboldi, Francesca Romana Grati, Giovanni Porta, Palma Finelli, Paolo Radice, Monica Miozzo

    Argitaratua 2009
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  7. 7
    Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis†

    Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis† nork Monica Miozzo, Carlo Selmi, Barbara Gentilin, Francesca Romana Grati, Silvia Maria Sirchia, Sabine Oertelt‐Prigione, Massimo Zuin, M. Eric Gershwin, Mauro Podda, Pietro Invernizzi

    Argitaratua 2007
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  8. 8
    Epigenetic modulation of the<i>IGF2</i>/<i>H19</i>imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction

    Epigenetic modulation of the<i>IGF2</i>/<i>H19</i>imprinted domain in human embryonic and extra-embryonic compartments and its possible role in fetal growth restriction nork Silvia Tabano, Patrizia Colapietro, Irene Cetin, Francesca Romana Grati, Susanna Zanutto, Chiara Mandò, Patrizio Antonazzo, P. Pileri, Franca Rossella, Lidia Larizza, Silvia Maria Sirchia, Monica Miozzo

    Argitaratua 2010
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  9. 9
    Loss of the Inactive X Chromosome and Replication of the Active X in <i>BRCA1</i>-Defective and Wild-type Breast Cancer Cells

    Loss of the Inactive X Chromosome and Replication of the Active X in <i>BRCA1</i>-Defective and Wild-type Breast Cancer Cells nork Silvia Maria Sirchia, Lisetta Ramoscelli, Francesca Romana Grati, Floriana Barbera, Danila Coradini, Franca Rossella, Giovanni Porta, Elena Lesma, Anna Ruggeri, Paolo Radice, Giuseppe Simoni, Monica Miozzo

    Argitaratua 2005
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  10. 10
    Performance of a targeted cell‐free<scp>DNA</scp>prenatal test for 22q11.2 deletion in a large clinical cohort

    Performance of a targeted cell‐free<scp>DNA</scp>prenatal test for 22q11.2 deletion in a large clinical cohort nork Elisa Bevilacqua, Jacques Jani, Rabih Chaoui, E.‐K. A. Suk, Ricardo Palma‐Dias, T.‐M. Ko, Steven L. Warsof, Renee Stokowski, Kohar Jones, Francesca Romana Grati, M. Schmid

    Argitaratua 2021
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  11. 11
    Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi

    Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi nork Francesca Romana Grati, Beatrice Grimi, Giuditia Frascoli, Anna Maria Di Meco, Rosaria Liuti, Silvia Milani, Anna Maria Trotta, Francesca Dulcetti, Enrico Grosso, Monica Miozzo, Federico Maggi, Giuseppe Simoni

    Argitaratua 2006
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  12. 12
    SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome

    SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome nork Cristina Gervasini, Francesca Romana Grati, Faustina Lalatta, Silvia Tabano, Barbara Gentilin, Patrizia Colapietro, Simona De Toffol, Giada Frontino, F. Motta, Silvia Maitz, Laura Bernardini, Bruno Dallapiccola, Luigi Fedele, Lidia Larizza, Monica Miozzo

    Argitaratua 2010
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  13. 13
    Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results

    Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results nork Francesca Romana Grati, Francesca Malvestiti, José Carlos Ferreira, Komal Bajaj, Elisa Gaetani, Cristina Agrati, Beatrice Grimi, Francesca Dulcetti, Anna Ruggeri, Simona De Toffol, Federico Maggi, Ronald J. Wapner, Susan J. Gross, Giuseppe Simoni

    Argitaratua 2014
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  14. 14
    X Chromosome Monosomy: A Common Mechanism for Autoimmune Diseases

    X Chromosome Monosomy: A Common Mechanism for Autoimmune Diseases nork Pietro Invernizzi, Monica Miozzo, Carlo Selmi, Luca Persani, Pier Maria Battezzati, Massimo Zuin, Simona Lucchi, Pier Luigi Meroni, Bianca Marasini, S. Zeni, Mitchell Watnik, Francesca Romana Grati, Giuseppe Simoni, M. Eric Gershwin, Mauro Podda

    Argitaratua 2005
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  15. 15
    Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA

    Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA nork Francesca Romana Grati, José Carlos Ferreira, Peter Benn, Claudia Izzi, Federica Verdi, E Vercellotti, Cristina Dalpiaz, Patrizia D’Ajello, Elisa Filippi, N. Volpe, Francesca Malvestiti, Federico Maggi, Giuseppe Simoni, T. Frusca, Gaetana Cirelli, Gabriella Bracalente, Antonino Lo Re, Daniela Surico, T. Ghi, Federico Prefumo

    Argitaratua 2019
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  16. 16
    Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

    Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 nork Antonio Novelli, Francesca Romana Grati, Lucia Ballarati, Laura Bernardini, Domenico Bizzoco, Lamberto Camurri, Rosario Casalone, L Cardarelli, Pietro Cavalli, Roberto Ciccone, M. Clementi, Leda Dalprà, Mattia Gentile, G Gelli, Paola Grammatico, Michela Malacarne, Anna Maria Nardone, Vanna Pecile, Giuseppe Simoni, Orsetta Zuffardi, Daniela Giardino

    Argitaratua 2012
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  17. 17
    Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions

    Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions nork Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, T. Blaine Crowley, Joanne C. Y. Loo, Lauren A. Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto García‐Miñaúr, M. Cristina Digilio, Bruno Marino, Beverly G. Coleman, Julie S. Moldenhauer, Anne S. Bassett, Donna M. McDonald‐McGinn

    Argitaratua 2023
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