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G Del Porto

Showing results (41-50 of 57) with videos related to

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Clinical Genetics|July 1, 1990
A male patient with 48,XXYY syndrome: importance of distinction from Klinefelter's syndromeP Grammatico, U Bottoni, S De Sanctis, et al.
Minerva Ginecologica|March 1, 1986
[Cytogenetic aspects of habitual abortion]G Del Porto, M Baldi, E D'Alessandro, et al.
International Journal of Cancer|April 15, 1989
Establishment and characterization of a human neuroblastoma cell lineS Scarpa, C Dominici, P Grammatico, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosisG Del Porto, E M Vingolo, K Steindl, et al.
Journal of Pediatric Surgery|August 2, 2003
Clinical management and molecular cytogenetic characterization in a 45,X/46,X,idic(Yp) patient with severe hypospadiaG Marrocco, M Poscente, S Majore, et al.
Cancer Genetics and Cytogenetics|April 1, 1990
Cytogenetic follow-up in a case of Sézary syndromeE D'Alessandro, P Paterlini, M L Lo Re, et al.
Cancer Genetics and Cytogenetics|January 1, 1992
Cytogenetic findings in terminal large cell transformation in a case of Sézary syndromeE D'Alessandro, A De Pasquale, C Ligas, et al.
Human Genetics|June 1, 1991
Paracentric inversion of chromosome 15(q15q24): description of three familiesE D'Alessandro, C De Matteis, M L Lo Re, et al.
Ophthalmology|September 1, 1996
Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observationsM R Pannarale, B Grammatico, A Iannaccone, et al.
Journal of Medical Genetics|September 1, 1994
Autosomal dominant simple microphthalmosE M Vingolo, K Steindl, R Forte, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Clinical Genetics|July 1, 1990
A male patient with 48,XXYY syndrome: importance of distinction from Klinefelter's syndromeP Grammatico, U Bottoni, S De Sanctis, et al.
Minerva Ginecologica|March 1, 1986
[Cytogenetic aspects of habitual abortion]G Del Porto, M Baldi, E D'Alessandro, et al.
International Journal of Cancer|April 15, 1989
Establishment and characterization of a human neuroblastoma cell lineS Scarpa, C Dominici, P Grammatico, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 1994
Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosisG Del Porto, E M Vingolo, K Steindl, et al.
Journal of Pediatric Surgery|August 2, 2003
Clinical management and molecular cytogenetic characterization in a 45,X/46,X,idic(Yp) patient with severe hypospadiaG Marrocco, M Poscente, S Majore, et al.
Cancer Genetics and Cytogenetics|April 1, 1990
Cytogenetic follow-up in a case of Sézary syndromeE D'Alessandro, P Paterlini, M L Lo Re, et al.
Cancer Genetics and Cytogenetics|January 1, 1992
Cytogenetic findings in terminal large cell transformation in a case of Sézary syndromeE D'Alessandro, A De Pasquale, C Ligas, et al.
Human Genetics|June 1, 1991
Paracentric inversion of chromosome 15(q15q24): description of three familiesE D'Alessandro, C De Matteis, M L Lo Re, et al.
Ophthalmology|September 1, 1996
Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observationsM R Pannarale, B Grammatico, A Iannaccone, et al.
Journal of Medical Genetics|September 1, 1994
Autosomal dominant simple microphthalmosE M Vingolo, K Steindl, R Forte, et al.
Pageof 6