Результаты поиска - Francesca Romana Grati
- Отображение 1 - 17 результаты of 17
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Genome‐wide non‐invasive prenatal screening for all cytogenetically visible imbalances по Peter Benn, Francesca Romana Grati
Опубликовано 2018Editorial -
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Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis† по Monica Miozzo, Carlo Selmi, Barbara Gentilin, Francesca Romana Grati, Silvia Maria Sirchia, Sabine Oertelt‐Prigione, Massimo Zuin, M. Eric Gershwin, Mauro Podda, Pietro Invernizzi
Опубликовано 2007Artigo -
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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 по 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
Опубликовано 2010Artigo -
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Loss of the Inactive X Chromosome and Replication of the Active X in <i>BRCA1</i>-Defective and Wild-type Breast Cancer Cells по 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
Опубликовано 2005Artigo -
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Performance of a targeted cell‐free<scp>DNA</scp>prenatal test for 22q11.2 deletion in a large clinical cohort по 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
Опубликовано 2021Artigo -
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Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi по 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
Опубликовано 2006Artigo -
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SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome по 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
Опубликовано 2010Artigo -
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Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results по 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
Опубликовано 2014Artigo -
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X Chromosome Monosomy: A Common Mechanism for Autoimmune Diseases по 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
Опубликовано 2005Artigo -
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Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA по 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
Опубликовано 2019Artigo -
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Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 по 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
Опубликовано 2012Revisão -
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Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions по 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
Опубликовано 2023Revisão
Инструменты поиска:
Связанные темы
Biology
Genetics
Gene
Fetus
Medicine
Pregnancy
Chromosome
Prenatal diagnosis
Aneuploidy
Karyotype
Cell-free fetal DNA
Chorionic villus sampling
Obstetrics
Amniocentesis
Internal medicine
X chromosome
Andrology
Chorionic villi
Chromosome abnormality
Trisomy
Cancer
Genetic counseling
Gynecology
Phenotype
Placenta
Uniparental disomy
Bioinformatics
Breast cancer
Cancer research
Chromosome 7 (human)