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Human Genetics|October 1, 1995
Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markersS Kytölä, J Leisti, R Winqvist, et al.Clinical Genetics|June 1, 1983
Marker X-associated mental retardation. A study of 150 retarded malesM Kähkönen, J Leisti, M Wilska, et al.Scandinavian Journal of Plastic and Reconstructive Surgery|January 1, 1980
Oblique facial clefts: case reportA Rintala, J Leisti, M Liesmaa, et al.Scandinavian Journal of Haematology|March 1, 1979
Hexokinase deficiency in erythrocytes: a new variant in 5 members of a Finnish familyM A Siimes, E L Rahiala, J LeistiJournal of Ocular Pharmacology|January 1, 1988
Timolol binding to bovine ocular melanin in vitroP Aula, T Kaila, R Huupponen, et al.The Journal of Biological Chemistry|September 10, 1983
Purification and properties of human hepatic aspartylglucosaminidaseM M McGovern, P Aula, R J DesnickThe Biochemical Journal|August 15, 1989
Isolation of a human hepatic 60 kDa aspartylglucosaminidase consisting of three non-identical polypeptidesM Baumann, L Peltonen, P Aula, et al.Clinical Genetics|September 1, 1986
Frequency of rare fragile sites among mentally subnormal schoolchildrenM Kähkönen, J Leisti, C J Thoden, et al.Journal of Medical Genetics|March 1, 1994
Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deteriorationA Hirvasniemi, H Lang, A E Lehesjoki, et al.Scandinavian Journal of Work, Environment & Health|April 1, 1984
Chromosome aberrations in lymphocytes of nurses handling cytostatic agentsE Nikula, K Kiviniitty, J Leisti, et al.Pageof 17