Showing results (91-100 of 185) with videos related to
Sort By:
Pageof 19
Human Genetics|February 1, 1993
Hypomelanosis of Ito in a girl with plexus papilloma and translocation (X;17)E Steichen-Gersdorf, R Trawöger, H C Duba, et al.Atherosclerosis|April 26, 1996
Lipoprotein(a) is increased in triglyceride-rich lipoproteins in men with coronary heart disease, but does not change acutely following oral fat ingestionF Hoppichler, H G Kraft, C Sandholzer, et al.Immunogenetics|October 31, 2001
High-resolution mapping of the human 4q21 and the mouse 5E3 SCYB chemokine cluster by fiber-fluorescence in situ hybridizationM Erdel, M Theurl, M Meyer, et al.Human Genetics|March 1, 1990
Frequency and effect of human apolipoprotein A-IV polymorphism on lipid and lipoprotein levels in an Icelandic populationH J Menzel, G Sigurdsson, E Boerwinkle, et al.Genes, Chromosomes & Cancer|March 10, 1998
Fluorescence in situ hybridization (FISH) on peripheral blood smears for monitoring Philadelphia chromosome-positive chronic myeloid leukemia (CML) during interferon treatment: a new strategy for remission assessmentJ Mühlmann, J Thaler, W Hilbe, et al.American Journal of Human Genetics|October 1, 1992
Lipoprotein(a) in women twins: heritability and relationship to apolipoprotein(a) phenotypesM A Austin, C Sandholzer, J V Selby, et al.The New England Journal of Medicine|May 24, 1990
Relation of serum lipoprotein(a) concentration and apolipoprotein(a) phenotype to coronary heart disease in patients with familial hypercholesterolemiaM Seed, F Hoppichler, D Reaveley, et al.Clinical Genetics|September 1, 1977
Studies on the metabolic defect in Broad-beta disease (hyperlipoproteinaemia type III)G Utermann, H Canzler, M Hees, et al.Cancer Genetics and Cytogenetics|May 18, 1999
Cytogenetic characterization of 22 human renal cell tumors in relation to a histopathological classificationI Verdorfer, A Hobisch, A Hittmair, et al.Journal of Medical Genetics|April 1, 1997
Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndromeH C Duba, M Erdel, J Löffler, et al.Pageof 19