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International Journal of Circumpolar Health|March 2, 2005
Cholestasis Familiaris Groenlandica/Byler-like disease in Greenland--a population studyH Eiberg, B Nørgaard-Pedersen, I M Nielsen
Human Genetics|February 1, 1992
Transferrin subtypes in 51 Danish patients with hereditary haemochromatosis and in 847 normal subjectsN Milman, H Eiberg, M Thymann, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Assignment of granular corneal dystrophy Groenouw type I (CDGG1) to chromosome 5qH Eiberg, H U Møller, I Berendt, et al.
Clinical Genetics|February 1, 1992
Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneityA M Lund, H Eiberg, T Rosenberg, et al.
Clinical Genetics|May 1, 1986
Linkage of transcobalamin II (TC2) to the P blood group system and assignment to chromosome 22H Eiberg, N Møller, J Mohr, et al.
Human Genetics|July 1, 1995
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36H Eiberg, A M Lund, M Warburg, et al.
The Journal of Urology|November 7, 2001
Linkage study of a large Danish 4-generation family with urge incontinence and nocturnal enuresisH Eiberg, H L Shaumburg, A Von Gontard, et al.
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