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G Novelli

Showing results (311-320 of 330) with videos related to

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Journal of Endocrinological Investigation|June 24, 2015
Characterization of endocrine features and genotype-phenotypes correlations in blepharophimosis-ptosis-epicanthus inversus syndrome type 1S Nuovo, M Passeri, E Di Benedetto, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|November 25, 2023
Are severity and location of facial trauma risk factors for cervical spine injuries? 10-year analysis based on the use of the AO spine injury classification and the comprehensive facial injury (CFI) scoreG Canzi, E De Ponti, A Spota, et al.
Human Mutation|July 17, 1999
Classical galactosemia and mutations at the galactose-1-phosphate uridyl transferase (GALT) geneL Tyfield, J Reichardt, J Fridovich-Keil, et al.
Eye (London, England)|September 16, 2017
Assessing individual risk for AMD with genetic counseling, family history, and genetic testingR Cascella, C Strafella, G Longo, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L)G Novelli, A Mari, F Amati, et al.
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
European Journal of Histochemistry : EJH|April 9, 2009
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
Transplantation Proceedings|February 1, 1996
Pediatric renal transplantation: personal experienceP Berloco, R Pretagostini, L Poli, et al.
European Journal of Histochemistry : EJH|September 27, 2018
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
American Journal of Human Genetics|April 1, 1996
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndromeA Pizzuti, G Novelli, A Mari, et al.
Pageof 33

Showing results (311-320 of 330) with videos related to

Sort By:
Pageof 33
Journal of Endocrinological Investigation|June 24, 2015
Characterization of endocrine features and genotype-phenotypes correlations in blepharophimosis-ptosis-epicanthus inversus syndrome type 1S Nuovo, M Passeri, E Di Benedetto, et al.
European Spine Journal : Official Publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society|November 25, 2023
Are severity and location of facial trauma risk factors for cervical spine injuries? 10-year analysis based on the use of the AO spine injury classification and the comprehensive facial injury (CFI) scoreG Canzi, E De Ponti, A Spota, et al.
Human Mutation|July 17, 1999
Classical galactosemia and mutations at the galactose-1-phosphate uridyl transferase (GALT) geneL Tyfield, J Reichardt, J Fridovich-Keil, et al.
Eye (London, England)|September 16, 2017
Assessing individual risk for AMD with genetic counseling, family history, and genetic testingR Cascella, C Strafella, G Longo, et al.
Biochimica Et Biophysica Acta|April 16, 1998
Structure and expression of the human ubiquitin fusion-degradation gene (UFD1L)G Novelli, A Mari, F Amati, et al.
American Journal of Human Genetics|June 12, 1999
Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11R Wadey, J McKie, C Papapetrou, et al.
European Journal of Histochemistry : EJH|April 9, 2009
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
Transplantation Proceedings|February 1, 1996
Pediatric renal transplantation: personal experienceP Berloco, R Pretagostini, L Poli, et al.
European Journal of Histochemistry : EJH|September 27, 2018
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
American Journal of Human Genetics|April 1, 1996
Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndromeA Pizzuti, G Novelli, A Mari, et al.
Pageof 33