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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.Human Molecular Genetics|October 1, 1992
Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotypeP Shelbourne, R Winqvist, E Kunert, et al.Human Genetics|October 1, 1990
Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish populationP Nokelainen, L Alanen-Kurki, R Winqvist, 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.Proceedings of the National Academy of Sciences of the United States of America|July 19, 1994
The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8E Tahvanainen, S Ranta, A Hirvasniemi, 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.Human Genetics|July 1, 1997
Human cationic amino acid transporter gene hCAT-2 is assigned to 8p22 but is not the causative gene in lysinuric protein intoleranceT Lauteala, N Horelli-Kuitunen, E Closs, et al.Nature Genetics|February 1, 1997
Characterization of the full fragile X syndrome mutation in fetal gametesH E Malter, J C Iber, R Willemsen, et al.Pageof 17