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International Journal of Oncology|November 18, 2000
Hypermetaphase and interphase fluorescence in situ hybridisation for monitoring of remission status in Philadelphia chromosome positive chronic myeloid leukaemiaH C Duba, W Hilbe, A Mehringer, et al.American Journal of Medical Genetics|April 15, 2000
Mental and psychomotoric retardation in two brothers with pure partial trisomy 7q32-q34 due to a maternal insertion (14;7)J Löffler, B Utermann, H C Duba, et al.Human Mutation|January 1, 1995
Apolipoprotein A-IV polymorphism in the Hungarian population: gene frequencies, effect on lipid levels, and sequence of two new variantsH J Menzel, H Dieplinger, C Sandholzer, et al.Human Genetics|May 1, 1990
Variation in the size of human apolipoprotein(a) is due to a hypervariable region in the geneG Lindahl, E Gersdorf, H J Menzel, et al.European Journal of Human Genetics : EJHG|October 22, 1998
Nail patella syndrome in a cytogenetically balanced t(9;17)(q34.1;q25) carrierH C Duba, M Erdel, J Löffler, et al.Kidney International|October 10, 1998
Influence of hematocrit on the measurement of lipoproteins demonstrated by the example of lipoprotein(a)F Kronenberg, E Trenkwalder, M F Kronenberg, et al.Journal of the American Veterinary Medical Association|August 1, 1978
Protein-losing enteropathy secondary to intestinal lymphangiectasia in a dogN C Olson, J F ZimmerMechanisms of Development|May 4, 2001
Protein kinase C isoenzyme: selective expression pattern of protein kinase C-θ during mouse developmentM Wilda, N Ghaffari-Tabrizi, I Reisert, et al.Ophthalmic Paediatrics and Genetics|March 1, 1986
Schnyder's dystrophy. Progression and metabolismW Lisch, E G Weidle, C Lisch, et al.Human Genetics|May 17, 2001
De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing lossA R Janecke, D Nekahm, J Löffler, et al.Pageof 19