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G Del Porto

Showing results (51-60 of 57) with videos related to

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Cancer Genetics and Cytogenetics|February 12, 1999
3p13 region: a possible location of a tumor suppressor gene involved in uveal melanomaM A Blasi, F Roccella, E Balestrazzi, et al.
World Journal of Surgery|May 1, 1995
Involvement of the 4q21 region in human malignant melanomas: cytogenetic and immunocytochemical characterization of three primary cell culturesP Grammatico, M Roccella, C Catricalà, et al.
Annali Italiani Di Chirurgia|July 1, 1995
[Gardner syndrome: diagnostic, clinical and genetic questions in the light of 2 case reports]S Messinetti, G Del Porto, L Giacomelli, et al.
Human Reproduction (Oxford, England)|May 1, 1993
Chromosome heteromorphisms and early recurrent abortionsG Del Porto, E D'Alessandro, P Grammatico, et al.
Human Genetics|October 1, 1988
Pericentric inversion of chromosome 19 in three familiesE D'Alessandro, C De Matteis Vaccarella, M L Lo Re, et al.
British Heart Journal|February 1, 1993
Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 familiesE Zachara, A L Caforio, G P Carboni, et al.
Human Mutation|January 29, 2000
Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. OnlineM G Miano, D Valverde, T Solans, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Cancer Genetics and Cytogenetics|February 12, 1999
3p13 region: a possible location of a tumor suppressor gene involved in uveal melanomaM A Blasi, F Roccella, E Balestrazzi, et al.
World Journal of Surgery|May 1, 1995
Involvement of the 4q21 region in human malignant melanomas: cytogenetic and immunocytochemical characterization of three primary cell culturesP Grammatico, M Roccella, C Catricalà, et al.
Annali Italiani Di Chirurgia|July 1, 1995
[Gardner syndrome: diagnostic, clinical and genetic questions in the light of 2 case reports]S Messinetti, G Del Porto, L Giacomelli, et al.
Human Reproduction (Oxford, England)|May 1, 1993
Chromosome heteromorphisms and early recurrent abortionsG Del Porto, E D'Alessandro, P Grammatico, et al.
Human Genetics|October 1, 1988
Pericentric inversion of chromosome 19 in three familiesE D'Alessandro, C De Matteis Vaccarella, M L Lo Re, et al.
British Heart Journal|February 1, 1993
Familial aggregation of idiopathic dilated cardiomyopathy: clinical features and pedigree analysis in 14 familiesE Zachara, A L Caforio, G P Carboni, et al.
Human Mutation|January 29, 2000
Two novel mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene in X-linked retinitis pigmentosa (RP3). Mutations in brief no. 172. OnlineM G Miano, D Valverde, T Solans, et al.
Pageof 6