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Cancer Genetics and Cytogenetics
|
February 12, 1999
3p13 region: a possible location of a tumor suppressor gene involved in uveal melanoma
M 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 cultures
P 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 abortions
G Del Porto, E D'Alessandro, P Grammatico, et al.
Human Genetics
|
October 1, 1988
Pericentric inversion of chromosome 19 in three families
E 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 families
E 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. Online
M G Miano, D Valverde, T Solans, et al.
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of 6
Search research articles
Search
Showing results (51-60 of 57) with videos related to
Sort By:
Page
of 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 melanoma
M 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 cultures
P 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 abortions
G Del Porto, E D'Alessandro, P Grammatico, et al.
Human Genetics
|
October 1, 1988
Pericentric inversion of chromosome 19 in three families
E 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 families
E 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. Online
M G Miano, D Valverde, T Solans, et al.
Page
of 6