Showing results (101-110 of 138) with videos related to
Sort By:
Pageof 14
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|September 14, 2000
Molecular genetics improves the management of hereditary non-polyposis colorectal cancerR S Ramesar, M V Madden, R Felix, et al.Blood|March 25, 2000
Delineation of a minimal interval and identification of 9 candidates for a tumor suppressor gene in malignant myeloid disorders on 5q31S K Horrigan, Z H Arbieva, H Y Xie, et al.The Journal of Invasive Cardiology|September 6, 2000
Timing of coronary stent thrombosis in patients treated with prophylactic tirofibanA R Assali, S Sdringola, M Ghani, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 31, 1999
N-linked glycan of a sperm CD52 glycoform associated with human infertilityA B Diekman, E J Norton, K L Klotz, et al.Genomics|April 7, 1999
A radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesS K Horrigan, L Bartoloni, M C Speer, et al.Oncogene|November 1, 2001
A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31Z Hu, I Gomes, S K Horrigan, et al.Science (New York, N.Y.)|October 26, 1990
Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridizationD C Tkachuk, C A Westbrook, M Andreeff, et al.Molecular Human Reproduction|October 3, 2006
Hominoid-specific SPANXA/D genes demonstrate differential expression in individuals and protein localization to a distinct nuclear envelope domain during spermatid morphogenesisV A Westbrook, P D Schoppee, G R Vanage, et al.Science (New York, N.Y.)|February 28, 1986
Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disordersM M Le Beau, C A Westbrook, M O Diaz, et al.Cytogenetics and Cell Genetics|January 1, 1994
Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme HumainC A Westbrook, M M Le Beau, W L Neuman, et al.Pageof 14