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A Iolascon

Showing results (91-100 of 154) with videos related to

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British Journal of Haematology|January 1, 1992
Hereditary spherocytosis characterized by increased spectrin/band 3 ratioE Miraglia del Giudice, S Perrotta, L Pinto, et al.
Leukemia|March 1, 1997
Frequent clonal loss of heterozygosity (LOH) in the chromosomal region 1p32 occurs in childhood T cell acute lymphoblastic leukemia (T-ALL) carrying rearrangements of the TAL1 geneA Iolascon, M F Faienza, B Coppola, et al.
International Journal of Oncology|May 17, 2011
Rare frequencey of point mutations for codon 12, 13 and 61 of ras gene in italian neuroblastomaA Iolascon, M Badiali, A Pession, et al.
European Journal of Haematology|June 8, 1999
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndromeA Iolascon, M F Faienza, L Giordani, et al.
British Journal of Haematology|June 1, 1996
P16INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9M F Faienza, F della Ragione, G Basso, et al.
British Journal of Cancer|March 29, 2000
Reduced expression of transforming growth factor-beta receptor type III in high stage neuroblastomasA Iolascon, L Giordani, A Borriello, et al.
Blood|September 15, 1996
Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemiaL Baronciani, A Zanella, P Bianchi, et al.
Oncogenesis|April 5, 2016
CD55 is a HIF-2α marker with anti-adhesive and pro-invading properties in neuroblastomaF Cimmino, M Avitabile, L Pezone, et al.
American Journal of Human Genetics|November 5, 1997
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchP Gasparini, E Miraglia del Giudice, J Delaunay, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Cytogenetic analysis of hepatoblastoma: hypothesis of cytogenetic evolution in such tumors and results of a multicentric studyL Sainati, A Leszl, M Stella, et al.
Pageof 16

Showing results (91-100 of 154) with videos related to

Sort By:
Pageof 16
British Journal of Haematology|January 1, 1992
Hereditary spherocytosis characterized by increased spectrin/band 3 ratioE Miraglia del Giudice, S Perrotta, L Pinto, et al.
Leukemia|March 1, 1997
Frequent clonal loss of heterozygosity (LOH) in the chromosomal region 1p32 occurs in childhood T cell acute lymphoblastic leukemia (T-ALL) carrying rearrangements of the TAL1 geneA Iolascon, M F Faienza, B Coppola, et al.
International Journal of Oncology|May 17, 2011
Rare frequencey of point mutations for codon 12, 13 and 61 of ras gene in italian neuroblastomaA Iolascon, M Badiali, A Pession, et al.
European Journal of Haematology|June 8, 1999
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndromeA Iolascon, M F Faienza, L Giordani, et al.
British Journal of Haematology|June 1, 1996
P16INK4A gene homozygous deletions in human acute leukaemias with alterations of chromosome 9M F Faienza, F della Ragione, G Basso, et al.
British Journal of Cancer|March 29, 2000
Reduced expression of transforming growth factor-beta receptor type III in high stage neuroblastomasA Iolascon, L Giordani, A Borriello, et al.
Blood|September 15, 1996
Study of the molecular defects in glucose phosphate isomerase-deficient patients affected by chronic hemolytic anemiaL Baronciani, A Zanella, P Bianchi, et al.
Oncogenesis|April 5, 2016
CD55 is a HIF-2α marker with anti-adhesive and pro-invading properties in neuroblastomaF Cimmino, M Avitabile, L Pezone, et al.
American Journal of Human Genetics|November 5, 1997
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide searchP Gasparini, E Miraglia del Giudice, J Delaunay, et al.
Cancer Genetics and Cytogenetics|July 2, 1998
Cytogenetic analysis of hepatoblastoma: hypothesis of cytogenetic evolution in such tumors and results of a multicentric studyL Sainati, A Leszl, M Stella, et al.
Pageof 16