Showing results (81-90 of 264) with videos related to

Sort By:
Pageof 27
Lancet (London, England)|February 22, 1975
Alpha-fetoprotein in antenatal diagnosis of congenital nephrosisB Kjessler, S G Johansson, M Sherman, et al.
Clinical Genetics|November 1, 1988
A new type of muscular dystrophy in two brothers: analysis by use of DNA probes suggests autosomal recessive inheritanceP Goonewardena, K H Gustavson, I Gamstorp, et al.
Hearing Research|August 1, 1996
Immunohistochemical localization of basement membrane collagens and associated proteins in the murine cochleaD Cosgrove, G Samuelson, J Pinnt
European Journal of Clinical Nutrition|December 10, 1998
Food habits in Swedish adolescents in relation to socioeconomic conditionsD Höglund, G Samuelson, A Mark
American Journal of Medical Genetics|February 1, 1991
Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304N Dahl, H Malmgren, U Pettersson, et al.
Acta Dermato-Venereologica|March 23, 1999
Further evidence of genetic homogeneity in Sjögren-Larsson syndromeM Pigg, I Annton-Lamprecht, C Braun-Quentin, et al.
Clinical Genetics|December 1, 1983
Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence studyH K Blomquist, K H Gustavson, G Holmgren, et al.
Acta Paediatrica Scandinavica|March 1, 1980
Zinc and immune function in Down's syndromeB Björkstén, O Bäck, K H Gustavson, et al.
European Journal of Human Genetics : EJHG|January 1, 1994
Strong founder effect for the fragile X syndrome in SwedenH Malmgren, K H Gustavson, C Oudet, et al.
Nature Genetics|December 1, 1994
The Sjögren-Larsson syndrome gene is close to D17S805 as determined by linkage analysis and allelic associationM Pigg, S Jagell, A Sillén, et al.
Pageof 27