Suchergebnisse - Francesca Romana Grati
- Treffer 1 - 17 von 17
-
1
Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis von Francesca Romana Grati
Veröffentlicht 2014Revisão -
2
-
3
Genome‐wide non‐invasive prenatal screening for all cytogenetically visible imbalances von Peter Benn, Francesca Romana Grati
Veröffentlicht 2018Editorial -
4
-
5
-
6
-
7
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosis† von Monica Miozzo, Carlo Selmi, Barbara Gentilin, Francesca Romana Grati, Silvia Maria Sirchia, Sabine Oertelt‐Prigione, Massimo Zuin, M. Eric Gershwin, Mauro Podda, Pietro Invernizzi
Veröffentlicht 2007Artigo -
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 von 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
Veröffentlicht 2010Artigo -
9
Loss of the Inactive X Chromosome and Replication of the Active X in <i>BRCA1</i>-Defective and Wild-type Breast Cancer Cells von 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
Veröffentlicht 2005Artigo -
10
Performance of a targeted cell‐free<scp>DNA</scp>prenatal test for 22q11.2 deletion in a large clinical cohort von 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
Veröffentlicht 2021Artigo -
11
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi von 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
Veröffentlicht 2006Artigo -
12
SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome von 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
Veröffentlicht 2010Artigo -
13
Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results von 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
Veröffentlicht 2014Artigo -
14
X Chromosome Monosomy: A Common Mechanism for Autoimmune Diseases von 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
Veröffentlicht 2005Artigo -
15
Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA von 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
Veröffentlicht 2019Artigo -
16
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 von 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
Veröffentlicht 2012Revisão -
17
Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions von 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
Veröffentlicht 2023Revisão
Suchwerkzeuge:
Ähnliche Schlagworte
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)