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A W Eriksson

Showing results (81-90 of 155) with videos related to

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Nordisk Medicin|December 3, 1970
[Qualitative and quantitative haptoglobin studies on the Finnish Lapps]A W Eriksson, M Kirjarinta, J Fellman, et al.
Nature|March 12, 1981
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemiaH Joenje, F Arwert, A W Eriksson, et al.
Acta Ophthalmologica Scandinavica|May 20, 1998
Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in FinlandH Forsius, M Damsten, A W Eriksson, et al.
American Journal of Human Genetics|January 1, 1991
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysisT Alitalo, T A Kruse, H Forsius, et al.
Humangenetik|January 1, 1971
Pseudocholinesterase polymorphism among Lapp populations in FinlandS Singh, M Jensen, H W Goedde, et al.
Clinical Genetics|June 1, 1980
Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinismF E O'Donnell, W R Green, V A McKusick, et al.
Annals of Human Biology|May 1, 1986
ABH secretion polymorphism in Icelanders, Aland Islanders, Finns, Finnish Lapps, Komi and Greenland Eskimos: a review and new dataA W Eriksson, K Partanen, R R Frants, et al.
Blood|July 1, 1983
Genetic evidence for fetal origin of transcobalamin II in human cord bloodH J Porck, M Fràter-Schröder, R R Frants, et al.
Human Heredity|January 1, 1974
Pseudocholinesterase polymorphism among alanders (Finno-Swedes), maris (Cheremisses, USSR) and greenland eskimos, and the segregation of some E1 and E2 locus types in Finnish Lapp FamiliesS Singh, K Saternus, H Münsch, et al.
Human Genetics|January 1, 1982
Evidence of duplication of the human salivary amylase geneJ C Pronk, R R Frants, W Jansen, et al.
Pageof 16

Showing results (81-90 of 155) with videos related to

Sort By:
Pageof 16
Nordisk Medicin|December 3, 1970
[Qualitative and quantitative haptoglobin studies on the Finnish Lapps]A W Eriksson, M Kirjarinta, J Fellman, et al.
Nature|March 12, 1981
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemiaH Joenje, F Arwert, A W Eriksson, et al.
Acta Ophthalmologica Scandinavica|May 20, 1998
Autosomal recessive cornea plana. A clinical and genetic study of 78 cases in FinlandH Forsius, M Damsten, A W Eriksson, et al.
American Journal of Human Genetics|January 1, 1991
Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysisT Alitalo, T A Kruse, H Forsius, et al.
Humangenetik|January 1, 1971
Pseudocholinesterase polymorphism among Lapp populations in FinlandS Singh, M Jensen, H W Goedde, et al.
Clinical Genetics|June 1, 1980
Forsius-Eriksson syndrome: its relation to the Nettleship-Falls X-linked ocular albinismF E O'Donnell, W R Green, V A McKusick, et al.
Annals of Human Biology|May 1, 1986
ABH secretion polymorphism in Icelanders, Aland Islanders, Finns, Finnish Lapps, Komi and Greenland Eskimos: a review and new dataA W Eriksson, K Partanen, R R Frants, et al.
Blood|July 1, 1983
Genetic evidence for fetal origin of transcobalamin II in human cord bloodH J Porck, M Fràter-Schröder, R R Frants, et al.
Human Heredity|January 1, 1974
Pseudocholinesterase polymorphism among alanders (Finno-Swedes), maris (Cheremisses, USSR) and greenland eskimos, and the segregation of some E1 and E2 locus types in Finnish Lapp FamiliesS Singh, K Saternus, H Münsch, et al.
Human Genetics|January 1, 1982
Evidence of duplication of the human salivary amylase geneJ C Pronk, R R Frants, W Jansen, et al.
Pageof 16