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G Novelli

Showing results (241-250 of 330) with videos related to

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Lancet (London, England)|December 9, 1989
Delta F508 gene deletion in cystic fibrosis in southern EuropeX Estivill, M Chillon, T Casals, et al.
American Journal of Human Genetics|May 1, 1992
A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentationV Nunes, A Bonizzato, A Gaona, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndromeF Amati, E Conti, A Novelli, et al.
Transplantation Proceedings|September 15, 2012
Glasgow coma score and tumor necrosis factor α as predictive criteria for initial poor graft functionG Novelli, V Morabito, Q Lai, et al.
Transplantation Proceedings|September 15, 2012
Preliminary study of early histomorphometric changes in hepatic steatosisF Marinozzi, S Novelli, V Morabito, et al.
Genomics|April 1, 1993
Identification of eight novel mutations in a collaborative analysis of a part of the second transmembrane domain of the CFTR geneB Mercier, W Lissens, G Novelli, et al.
Human Mutation|January 1, 1996
Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locusF Capon, C Levato, E Bussaglia, et al.
Human Genetics|October 1, 1991
Analysis of 14 cystic fibrosis mutations in five south European populationsV Nunes, P Gasparini, G Novelli, et al.
Neuropathology and Applied Neurobiology|January 28, 2010
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' musclesR Massa, M B Panico, S Caldarola, et al.
The Journal of Investigative Dermatology|May 12, 2001
Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21F Capon, S Semprini, S Chimenti, et al.
Pageof 33

Showing results (241-250 of 330) with videos related to

Sort By:
Pageof 33
Lancet (London, England)|December 9, 1989
Delta F508 gene deletion in cystic fibrosis in southern EuropeX Estivill, M Chillon, T Casals, et al.
American Journal of Human Genetics|May 1, 1992
A frameshift mutation (2869insG) in the second transmembrane domain of the CFTR gene: identification, regional distribution, and clinical presentationV Nunes, A Bonizzato, A Gaona, et al.
European Journal of Human Genetics : EJHG|December 22, 1999
Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndromeF Amati, E Conti, A Novelli, et al.
Transplantation Proceedings|September 15, 2012
Glasgow coma score and tumor necrosis factor α as predictive criteria for initial poor graft functionG Novelli, V Morabito, Q Lai, et al.
Transplantation Proceedings|September 15, 2012
Preliminary study of early histomorphometric changes in hepatic steatosisF Marinozzi, S Novelli, V Morabito, et al.
Genomics|April 1, 1993
Identification of eight novel mutations in a collaborative analysis of a part of the second transmembrane domain of the CFTR geneB Mercier, W Lissens, G Novelli, et al.
Human Mutation|January 1, 1996
Deletion analysis of the simple tandem repeat loci physically linked to the spinal muscular atrophy locusF Capon, C Levato, E Bussaglia, et al.
Human Genetics|October 1, 1991
Analysis of 14 cystic fibrosis mutations in five south European populationsV Nunes, P Gasparini, G Novelli, et al.
Neuropathology and Applied Neurobiology|January 28, 2010
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' musclesR Massa, M B Panico, S Caldarola, et al.
The Journal of Investigative Dermatology|May 12, 2001
Fine mapping of the PSORS4 psoriasis susceptibility region on chromosome 1q21F Capon, S Semprini, S Chimenti, et al.
Pageof 33