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Silvia Russo

Showing results (81-90 of 159) with videos related to

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Human Molecular Genetics|April 2, 2003
Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletionsGiorgio Gimelli, Miguel Angel Pujana, Maria Grazia Patricelli, et al.
Italian Journal of Pediatrics|September 28, 2024
A long way to syndromic short statureFederica Gaudioso, Camilla Meossi, Lidia Pezzani, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutationsMauro Longoni, Silvia Moncini, Mariangela Cisternino, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 22, 2024
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndromeFrancesca Cogliati, Letizia Straniero, Valeria Rimoldi, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Prevalence of Beckwith-Wiedemann syndrome in North West of ItalyAlessandro Mussa, Silvia Russo, Agostina De Crescenzo, et al.
Annali Dell'Istituto Superiore Di Sanita|June 17, 2026
External quality assessment programs in cytogenomics in the Lombardy Region, Italy (2018-2024): performance and trendsFabio Pasotti, Valentina Achille, Simona Da Molin, et al.
American Journal of Physiology. Cell Physiology|January 24, 2025
Dysfunctional mitochondrial bioenergetics sustains drug resistance in cancer cellsDavide Gnocchi, Dragana Nikolic, Silvia Russo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 28, 2015
Antiepileptic drugs in Rett SyndromeMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrumCristina Gervasini, Silvia Russo, Anna Cereda, et al.
Scientific Reports|December 22, 2025
PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletionAlessandro Vimercati, Giuseppa Patti, Pierpaola Tannorella, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|April 2, 2003
Genomic inversions of human chromosome 15q11-q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletionsGiorgio Gimelli, Miguel Angel Pujana, Maria Grazia Patricelli, et al.
Italian Journal of Pediatrics|September 28, 2024
A long way to syndromic short statureFederica Gaudioso, Camilla Meossi, Lidia Pezzani, et al.
American Journal of Medical Genetics. Part A|August 5, 2010
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutationsMauro Longoni, Silvia Moncini, Mariangela Cisternino, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 22, 2024
Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndromeFrancesca Cogliati, Letizia Straniero, Valeria Rimoldi, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Prevalence of Beckwith-Wiedemann syndrome in North West of ItalyAlessandro Mussa, Silvia Russo, Agostina De Crescenzo, et al.
Annali Dell'Istituto Superiore Di Sanita|June 17, 2026
External quality assessment programs in cytogenomics in the Lombardy Region, Italy (2018-2024): performance and trendsFabio Pasotti, Valentina Achille, Simona Da Molin, et al.
American Journal of Physiology. Cell Physiology|January 24, 2025
Dysfunctional mitochondrial bioenergetics sustains drug resistance in cancer cellsDavide Gnocchi, Dragana Nikolic, Silvia Russo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 28, 2015
Antiepileptic drugs in Rett SyndromeMaria Pintaudi, Maria Grazia Calevo, Aglaia Vignoli, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrumCristina Gervasini, Silvia Russo, Anna Cereda, et al.
Scientific Reports|December 22, 2025
PEG10 loss of function causes Silver-Russell syndrome: a familial case with paternal deletionAlessandro Vimercati, Giuseppa Patti, Pierpaola Tannorella, et al.
Pageof 16