Showing results (51-60 of 250) with videos related to
Sort By:
Pageof 25
Bioinformatics (Oxford, England)|April 25, 2015
MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studiesD Vuckovic, P Gasparini, N Soranzo, et al.Blood Cells, Molecules & Diseases|January 10, 2002
Linkage to chromosome 1q in Greek families with juvenile hemochromatosisG Papanikolaou, M Politou, A Roetto, et al.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.American Journal of Medical Genetics|January 20, 1997
Limb-pelvis hypoplasia/aplasia: a discrete entity in the fibuloulnar developmental field complexM Genuardi, P Gasparini, G Neri, et al.La Clinica Terapeutica|November 30, 1990
[Severe ventricular arrhythmia secondary to indapamide-induced hypopotassemia]F Guzzini, R Baroffio, D Coppetti, et al.Genomics|August 1, 1991
High conservation of sequences involved in cystic fibrosis mutations in five mammalian speciesP Gasparini, V Nunes, M Dognini, 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.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.Pageof 25