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Author/Creator Soli, Fiorenza

1. Characterization of intellectual disability and autism comorbidity through gene panel sequencing. Issue 6 (20th March 2020)

Authors:
Aspromonte, Maria C.; Bellini, Mariagrazia; Gasparini, Alessandra; Carraro, Marco; Bettella, Elisa; Polli, Roberta; Cesca, Federica; Bigoni, Stefania; Boni, Stefania; Carlet, Ombretta; Negrin, Susanna; Mammi, Isabella; Milani, Donatella; Peron, Angela; Sartori, Stefano; Toldo, Irene; Soli, Fioren...
Journal:
Human mutation
Issue:
Volume 41:Issue 6(2020)
Page Start:
1183
Record Type:
Journal Article
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2. Characterization of intellectual disability and autism comorbidity through gene panel sequencing. Issue 9 (2nd August 2019)

Authors:
Aspromonte, Maria C.; Bellini, Mariagrazia; Gasparini, Alessandra; Carraro, Marco; Bettella, Elisa; Polli, Roberta; Cesca, Federica; Bigoni, Stefania; Boni, Stefania; Carlet, Ombretta; Negrin, Susanna; Mammi, Isabella; Milani, Donatella; Peron, Angela; Sartori, Stefano; Toldo, Irene; Soli, Fioren...
Editors:
Moult, John; Brenner, Steven E.
Other Names:
Karchin Rachel guestEditor.; Pal Lipika R. specialEditor.
Journal:
Human mutation
Issue:
Volume 40:Issue 9(2019)
Page Start:
1346
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I. Issue 1 (3rd September 2021)

Authors:
Riva, Matteo; Martorana, Davide; Uliana, Vera; Caleffi, Edoardo; Boschi, Elena; Garavelli, Livia; Ponti, Giovanni; Sangiorgi, Luca; Graziano, Claudio; Bigoni, Stefania; Rocchetti, Luca Maria; Madeo, Simona; Soli, Fiorenza; Grosso, Enrico; Carli, Diana; Goldoni, Matteo; Pisani, Francesco; Percesep...
Journal:
Genes, chromosomes & cancer
Issue:
Volume 61:Issue 1(2022)
Page Start:
10
Record Type:
Journal Article
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5. Small supernumerary marker chromosomes: A legacy of trisomy rescue?. Issue 2 (22nd November 2018)

Authors:
Kurtas, Nehir Edibe; Xumerle, Luciano; Leonardelli, Lorena; Delledonne, Massimo; Brusco, Alfredo; Chrzanowska, Krystyna; Schinzel, Albert; Larizza, Daniela; Guerneri, Silvana; Natacci, Federica; Bonaglia, Maria Clara; Reho, Paolo; Manolakos, Emmanouil; Mattina, Teresa; Soli, Fiorenza; Provenzano,...
Journal:
Human mutation
Issue:
Volume 40:Issue 2(2019)
Page Start:
193
Record Type:
Journal Article
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