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Hereditas|June 12, 1999
Characterization of the lysinuric protein intolerance (LPI) region within T-cell receptor alpha/delta gene cluster on chromosome site 14q11T Lauteala, J Mykkänen, N Horelli-Kuitunen, et al.Journal of Medical Genetics|May 1, 1990
X linked neonatal myotubular myopathy: one recombination detected with four polymorphic DNA markers from Xq28A E Lehesjoki, E M Sankila, J Miao, et al.Neuropediatrics|October 1, 1994
Phenotypic variation and magnetic resonance imaging (MRI) in Salla disease, a free sialic acid storage disorderL Haataja, R Parkkola, P Sonninen, et al.Kidney International|August 31, 2006
Glomerular sclerosis in kidneys with congenital nephrotic syndrome (NPHS1)A-M Kuusniemi, J Merenmies, A-T Lahdenkari, et al.Lancet (London, England)|April 13, 1996
Prenatal diagnosis of Batten's diseaseP B Munroe, J Rapola, H M Mitchison, et al.Atherosclerosis|August 1, 1988
Effect of repeated endotoxin treatment and hypercholesterolemia on preatherosclerotic lesions in weaned pigs. Part II. Lipid and glycosaminoglycan analysis of intima and inner mediaS Ylä-Herttuala, E Pesonen, E Kaprio, et al.Kidney International|October 1, 1993
Post-transplantation nephrosis in congenital nephrotic syndrome of the Finnish typeJ Laine, H Jalanko, H Holthöfer, et al.American Journal of Human Genetics|June 1, 1994
The genetic locus for free sialic acid storage disease maps to the long arm of chromosome 6L Haataja, J Schleutker, A P Laine, et al.Parasitology|August 25, 2020
Molecular identification of Ancylostoma ceylanicum in the PhilippinesOyime P Aula, Donald P McManus, Kosala G Weerakoon, et al.European Journal of Human Genetics : EJHG|January 15, 1999
Genetic homogeneity of lysinuric protein intoleranceT Lauteala, J Mykkänen, M P Sperandeo, et al.Pageof 27