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Prenatal Diagnosis|July 28, 2015
Interpreting mosaicism in chorionic villi: results of a monocentric series of 1001 mosaics in chorionic villi with follow-up amniocentesisFrancesca Malvestiti, Cristina Agrati, Beatrice Grimi, et al.
European Journal of Human Genetics : EJHG|January 19, 2006
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villiFrancesca R Grati, Beatrice Grimi, Giuditia Frascoli, et al.
Fetal Diagnosis and Therapy|October 24, 2018
Risk of Fetal Loss in Pregnancies Undergoing Midtrimester Amniocentesis after Inconclusive Chorionic Villus SamplingGinevra Salsi, Francesca Romana Grati, Federica Bellussi, et al.
Case Reports in Genetics|June 14, 2013
Recombinant chromosome 4 from a familial pericentric inversion: prenatal and adulthood wolf-hirschhorn phenotypesFrancesca Malvestiti, Francesco Benedicenti, Simona De Toffol, et al.
Prenatal Diagnosis|October 23, 2016
Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high-risk indicationsJose Carlos P Ferreira, Francesca R Grati, Komal Bajaj, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Pure monosomy and pure trisomy of 13q21.2-31.1 consequent to a familial insertional translocation: exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)Francesca R Grati, Marci M Lesperance, Simona De Toffol, et al.
Nature Food|November 1, 2025
Identifying the safe operating space for food systemsSofie Te Wierik, Fabrice DeClerck, Arthur Beusen, et al.
Molecular and Cellular Probes|July 29, 2008
Prenatal detection by subtelomeric FISH and MLPA of unbalanced meiotic recombinants resulting from parental pericentric inversionsFrancesca R Grati, Sara Chinetti, Roberta Malgara, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 15, 2014
Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening resultsFrancesca R Grati, Francesca Malvestiti, Jose C P B Ferreira, et al.
Prenatal Diagnosis|January 18, 2014
De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approachesFrancesca Malvestiti, Simona De Toffol, Beatrice Grimi, et al.
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