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First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study.
Published in:
2020
By:
- Kagan, Karl Oliver;
- Hoopmann, Markus;
- Pfaff, Theresa;
- Prodan, Natalia;
- Wagner, Philipp;
- Schmid, Maximilian;
- Dufke, Andreas;
- Mau-Holzmann, Ulrike;
- Brucker, Sara;
- Marcato, Livia;
- Malvestiti, Barbara;
- Grati, Francesca Romana
Publication type:
journal article
Pregnancy on dialysis and with a failing kidney graft: A double challenge for non-invasive prenatal testing.
Published in:
2020
By:
- Attini, Rossella;
- Grati, Francesca R.;
- Menato, Guido;
- Todros, Tullia;
- Colla, Loredana;
- Rossetti, Maura;
- Malvestiti, Barbara;
- Alemanno, Maria G.;
- Masturzo, Bianca;
- Piccoli, Giorgina B.;
- Viora, Elsa
Publication type:
Case Study
Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
Published in:
2017
By:
- Grati, Francesca Romana;
- Bajaj, Komal;
- Zanatta, Valentina;
- Malvestiti, Francesca;
- Malvestiti, Barbara;
- Marcato, Livia;
- Grimi, Beatrice;
- Maggi, Federico;
- Simoni, Giuseppe;
- Gross, Susan J.;
- Ferreira, Jose
Publication type:
journal article
The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.
Published in:
2015
By:
- Grati, Francesca Romana;
- Bajaj, Komal;
- Malvestiti, Francesca;
- Agrati, Cristina;
- Grimi, Beatrice;
- Malvestiti, Barbara;
- Pompilii, Eva;
- Maggi, Federico;
- Gross, Susan;
- Simoni, Giuseppe;
- Ferreira, Jose Carlos P.
Publication type:
journal article
Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Published in:
Prenatal Diagnosis, 2015, v. 35, n. 8, p. 801, doi. 10.1002/pd.4613
By:
- Grati, Francesca Romana;
- Molina Gomes, Denise;
- Ferreira, Jose Carlos Pinto B.;
- Dupont, Celine;
- Alesi, Viola;
- Gouas, Laetitia;
- Horelli‐Kuitunen, Nina;
- Choy, Kwong Wai;
- García‐Herrero, Sandra;
- Vega, Alberto Gonzalez;
- Piotrowski, Krzysztof;
- Genesio, Rita;
- Queipo, Gloria;
- Malvestiti, Barbara;
- Hervé, Bérénice;
- Benzacken, Brigitte;
- Novelli, Antonio;
- Vago, Philippe;
- Piippo, Kirsi;
- Leung, Tak Yeung
Publication type:
Article
De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.
Published in:
Prenatal Diagnosis, 2014, v. 34, n. 5, p. 460, doi. 10.1002/pd.4330
By:
- Malvestiti, Francesca;
- De Toffol, Simona;
- Grimi, Beatrice;
- Chinetti, Sara;
- Marcato, Livia;
- Agrati, Cristina;
- Di Meco, Anna Maria;
- Frascoli, Giuditta;
- Trotta, Anna;
- Malvestiti, Barbara;
- Ruggeri, Anna;
- Dulcetti, Francesca;
- Maggi, Federico;
- Simoni, Giuseppe;
- Grati, Francesca Romana
Publication type:
Article

Found: 6

First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study.

Pregnancy on dialysis and with a failing kidney graft: A double challenge for non-invasive prenatal testing.

Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.

The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.

De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.