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Acta Paediatrica (Oslo, Norway : 1992). Supplement|August 1, 1993
Early child health in Lahore, Pakistan: II. InbreedingM Yaqoob, K H Gustavson, F Jalil, et al.Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Achondroplasia in Sweden caused by the G1138A mutation in FGFR3A Alderborn, M Anvret, K H Gustavson, et al.Molecular and Chemical Neuropathology|August 1, 1991
Monoaminergic dysfunction in Sjögren-Larsson syndromeP Wester, U Bergström, A Brun, et al.Clinical Genetics|July 1, 1990
Abnormalities of the cerebellum in oro-facio-digital syndrome II (Mohr syndrome)G Annerén, K H Gustavson, S Jòzwiak, et al.Acta Paediatrica Scandinavica|July 1, 1985
Selenium in plasma and erythrocytes in patients with Down's syndrome and healthy controls. Variation in relation to age, sex and glutathione peroxidase activity in erythrocytesG Annerén, M Gebre-Medhin, K H Gustavson, et al.Journal of Child Neurology|August 2, 2000
D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boyO Eeg-Olofsson, W W Zhang, Y Olsson, et al.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.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.Pageof 14