Showing results (31-40 of 107) with videos related to

Sort By:
Pageof 11
Haematologica|November 1, 1990
Screening of beta-thalassemia mutations by PCR and ASO analysis in an Italian population of mixed geographic originA Alfarano, E Gottardi, A Serra, et al.
Genomics|September 1, 1991
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatchI Dianzani, C Camaschella, G Saglio, et al.
British Journal of Haematology|April 12, 2000
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteinsC Camaschella, G Zecchina, G Lockitch, et al.
Human Genetics|April 1, 1996
Allelic association of microsatellites of 6p in Italian hemochromatosis patientsC Camaschella, A Roetto, P Gasparini, et al.
Cancer|October 15, 1983
Increased proportion of suppressor/cytotoxic (OKT8+) cells in patients with Hodgkin's disease in long-lasting remissionF Lauria, R Foa, M Gobbi, et al.
Blood|August 1, 1987
The 3' ends of the deletions of Spanish delta beta zero-thalassemia and black HPFH 1 and 2 lie within 17 kilobasesC Camaschella, A Serra, G Saglio, et al.
Blood|November 26, 1999
Defective recovery and severe renal damage after acute hemolysis in hemopexin-deficient miceE Tolosano, E Hirsch, E Patrucco, et al.
Blood|February 15, 1990
A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancerC Camaschella, A Serra, E Gottardi, et al.
Haematologica|January 1, 1990
Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysisE Gottardi, A Alfarano, A Serra, et al.
Molecular and Cellular Probes|October 1, 1993
Construction of a genetic map telomeric to HLA-A by microsatellite analysisC Camaschella, A Roetto, G De Sandre, et al.
Pageof 11