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A Iolascon

Showing results (51-60 of 154) with videos related to

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Journal of Medical Genetics|August 28, 1999
21-Hydroxylase deficiency in Italy: a distinct distribution pattern of CYP21 mutations in a sample from southern ItalyA Bobba, E Marra, S Giannattasio, et al.
Hepatology (Baltimore, Md.)|April 16, 1998
Analysis of CDKN2A, CDKN2B, CDKN2C, and cyclin Ds gene status in hepatoblastomaA Iolascon, L Giordani, A Moretti, et al.
British Journal of Haematology|November 1, 1995
High frequency of homozygous deletions of CDK4I gene in childhood acute lymphoblastic leukaemiaA Iolascon, M F Faienza, B Coppola, et al.
Gut|September 21, 2007
Elevated expression and polymorphisms of SOCS3 influence patient response to antiviral therapy in chronic hepatitis CM Persico, M Capasso, R Russo, et al.
Leukemia|February 1, 1996
Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemiasA Iolascon, M F Faienza, B Coppola, et al.
Acta Haematologica|January 1, 1995
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian childS Gangarossa, V Romano, E Miraglia del Giudice, et al.
La Pediatria|January 1, 1983
[Campylobacter enteritis: an emerging disease]L Pinto, I Alagia, P Imparato, et al.
Blood|September 25, 1999
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosisE M del Giudice, S Perrotta, B Nobili, et al.
Haematologica|November 24, 1998
Expression of cell cycle regulatory genes in chronic myelogenous leukemiaA Iolascon, F Della Ragione, L Giordani, et al.
Haematologica|November 1, 1996
Congenital dyserythropoietic anemia type II: molecular basis and clinical aspectsA Iolascon, G D'Agostaro, S Perrotta, et al.
Pageof 16

Showing results (51-60 of 154) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|August 28, 1999
21-Hydroxylase deficiency in Italy: a distinct distribution pattern of CYP21 mutations in a sample from southern ItalyA Bobba, E Marra, S Giannattasio, et al.
Hepatology (Baltimore, Md.)|April 16, 1998
Analysis of CDKN2A, CDKN2B, CDKN2C, and cyclin Ds gene status in hepatoblastomaA Iolascon, L Giordani, A Moretti, et al.
British Journal of Haematology|November 1, 1995
High frequency of homozygous deletions of CDK4I gene in childhood acute lymphoblastic leukaemiaA Iolascon, M F Faienza, B Coppola, et al.
Gut|September 21, 2007
Elevated expression and polymorphisms of SOCS3 influence patient response to antiviral therapy in chronic hepatitis CM Persico, M Capasso, R Russo, et al.
Leukemia|February 1, 1996
Homozygous deletions of cyclin-dependent kinase inhibitor genes, p16(INK4A) and p18, in childhood T cell lineage acute lymphoblastic leukemiasA Iolascon, M F Faienza, B Coppola, et al.
Acta Haematologica|January 1, 1995
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian childS Gangarossa, V Romano, E Miraglia del Giudice, et al.
La Pediatria|January 1, 1983
[Campylobacter enteritis: an emerging disease]L Pinto, I Alagia, P Imparato, et al.
Blood|September 25, 1999
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosisE M del Giudice, S Perrotta, B Nobili, et al.
Haematologica|November 24, 1998
Expression of cell cycle regulatory genes in chronic myelogenous leukemiaA Iolascon, F Della Ragione, L Giordani, et al.
Haematologica|November 1, 1996
Congenital dyserythropoietic anemia type II: molecular basis and clinical aspectsA Iolascon, G D'Agostaro, S Perrotta, et al.
Pageof 16