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Alberto Sensi

Showing results (11-20 of 17) with videos related to

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Gene|May 16, 2019
Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disordersPamela Magini, Emanuela Scarano, Ilaria Donati, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversionMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.
Molecular Genetics & Genomic Medicine|December 28, 2020
Deciphering the pathogenesis of the COL4-related hematuric nephritis: A genotype/phenotype studyVera Uliana, Paola Sebastio, Matteo Riva, et al.
Journal of Human Genetics|May 30, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotypeFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Blood Advances|October 19, 2020
Gene expression profile predicts response to the combination of tosedostat and low-dose cytarabine in elderly AMLGiuseppe Visani, Federica Loscocco, Mike Dennis, et al.
Frontiers in Genetics|January 10, 2019
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number VariationsAnna Morgan, Stefania Lenarduzzi, Stefania Cappellani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2010
A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parentsMonica Marini, Renata Bocciardi, Stefania Gimelli, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Gene|May 16, 2019
Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disordersPamela Magini, Emanuela Scarano, Ilaria Donati, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversionMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.
Molecular Genetics & Genomic Medicine|December 28, 2020
Deciphering the pathogenesis of the COL4-related hematuric nephritis: A genotype/phenotype studyVera Uliana, Paola Sebastio, Matteo Riva, et al.
Journal of Human Genetics|May 30, 2020
Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotypeFederica Cesca, Elisa Bettella, Roberta Polli, et al.
Blood Advances|October 19, 2020
Gene expression profile predicts response to the combination of tosedostat and low-dose cytarabine in elderly AMLGiuseppe Visani, Federica Loscocco, Mike Dennis, et al.
Frontiers in Genetics|January 10, 2019
Genomic Studies in a Large Cohort of Hearing Impaired Italian Patients Revealed Several New Alleles, a Rare Case of Uniparental Disomy (UPD) and the Importance to Search for Copy Number VariationsAnna Morgan, Stefania Lenarduzzi, Stefania Cappellani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2010
A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parentsMonica Marini, Renata Bocciardi, Stefania Gimelli, et al.
Pageof 2