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Human Heredity|January 1, 1984
Spatial distribution of the gene for infantile genetic agranulocytosisL Iselius, K H GustavsonHuman Genetics|January 1, 1984
The mode of inheritance of psoriasis: evidence for a major gene as well as a multifactorial component and its implication for genetic counsellingL Iselius, W R WilliamsClinical Genetics|September 1, 1980
Genetic susceptibility to multiple sclerosis: a linkage analysis with age-of-onset correctionsR W Haile, S E Hodge, B R Visscher, et al.Clinical Pharmacokinetics|November 1, 1983
Formal genetics of isoniazid metabolism in manL Iselius, D A EvansJournal of Inherited Metabolic Disease|January 1, 1994
Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotesE Svensson, L Iselius, L HagenfeldtAmerican Journal of Human Genetics|May 1, 1981
Some epistatic two-locus models of disease. I. Relative risks and identity-by-descent distributions in affected sib pairsS E HodgeGenetic Epidemiology|January 1, 1995
An oliogenic disease displaying weak marker associations: a summary of contributions to problem 1 of GAW9S E HodgeAmerican Journal of Human Genetics|October 1, 1988
Conditioning on subsets of the data: applications to ascertainment and other genetic problemsS E HodgeAmerican Journal of Medical Genetics|March 26, 1998
Exact elods and exact power for affected sib pairs analyzed for linkage under simple right and wrong modelsS E HodgeAmerican Journal of Human Genetics|August 1, 1993
Linkage analysis versus association analysis: distinguishing between two models that explain disease-marker associationsS E HodgePageof 24