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M Seri

Showing results (31-40 of 73) with videos related to

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Nephron|January 1, 1994
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chainA Renieri, M Meroni, A Sessa, et al.
International Journal of Cancer|April 1, 1993
Epstein-Barr virus and gastric cancer: data and unanswered questionsL Leoncini, C Vindigni, T Megha, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1994
De-novo COL4A5 gene mutations in Alport's syndromeL Massella, G Rizzoni, R De Blasis, et al.
Nature|January 27, 1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseG Romeo, P Ronchetto, Y Luo, et al.
Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.
Oncogene|October 1, 1994
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogeneI Ceccherini, R M Hofstra, Y Luo, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Molecular cloning and mapping of a human cDNA (PA2G4) that encodes a protein highly homologous to the mouse cell cycle protein p38-2G4J Lamartine, M Seri, R Cinti, et al.
Journal of Internal Medicine|July 29, 1998
Association of multiple endocrine neoplasia type 2 and Hirschsprung diseaseG Romeo, I Ceccherini, J Celli, et al.
Molecular Syndromology|March 5, 2011
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic PhenotypeA Wischmeijer, P Magini, R Giorda, et al.
Neurogenetics|July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndromeA Catania, R Battini, T Pippucci, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Nephron|January 1, 1994
Variability of clinical phenotype in a large Alport family with Gly 1143 Ser change of collagen alpha 5(IV)-chainA Renieri, M Meroni, A Sessa, et al.
International Journal of Cancer|April 1, 1993
Epstein-Barr virus and gastric cancer: data and unanswered questionsL Leoncini, C Vindigni, T Megha, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1994
De-novo COL4A5 gene mutations in Alport's syndromeL Massella, G Rizzoni, R De Blasis, et al.
Nature|January 27, 1994
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseG Romeo, P Ronchetto, Y Luo, et al.
Human Genetics|October 1, 1993
Small frameshift deletions within the COL4A5 gene in juvenile-onset Alport syndromeA Renieri, M Seri, L Galli, et al.
Oncogene|October 1, 1994
DNA polymorphisms and conditions for SSCP analysis of the 20 exons of the ret proto-oncogeneI Ceccherini, R M Hofstra, Y Luo, et al.
Cytogenetics and Cell Genetics|January 1, 1997
Molecular cloning and mapping of a human cDNA (PA2G4) that encodes a protein highly homologous to the mouse cell cycle protein p38-2G4J Lamartine, M Seri, R Cinti, et al.
Journal of Internal Medicine|July 29, 1998
Association of multiple endocrine neoplasia type 2 and Hirschsprung diseaseG Romeo, I Ceccherini, J Celli, et al.
Molecular Syndromology|March 5, 2011
Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic PhenotypeA Wischmeijer, P Magini, R Giorda, et al.
Neurogenetics|July 5, 2018
R106C TFG variant causes infantile neuroaxonal dystrophy "plus" syndromeA Catania, R Battini, T Pippucci, et al.
Pageof 8