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American Journal of Medical Genetics|February 1, 1991
Fragile X families in a northern Swedish county: a genealogical study of possibly affected individuals in the nineteenth centuryU Drugge, H K Blomquist, K H Gustavson, et al.
American Journal of Medical Genetics|May 1, 1988
Fragile X families in a northern Swedish county--a genealogical study demonstrating apparent paternal transmission from the 18th centuryG Holmgren, H K Blomquist, U Drugge, et al.
Acta Paediatrica Scandinavica|January 1, 1991
Low concentrations of sodium and magnesium in erythrocytes from cystic fibrosis heterozygotesT Foucard, M Gebre-Medhin, K H Gustavson, et al.
Upsala Journal of Medical Sciences. Supplement|January 1, 1987
DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3P Goonewardena, N Dahl, K H Gustavson, et al.
Dermatologica|January 1, 1979
Pustulosis palmoplantaris and its relation to chronic recurrent multifocal osteomyelitisK Bergdahl, B Björkstén, K H Gustavson, et al.
The Journal of Pediatrics|August 1, 1978
Chronic recurrent multifocal osteomyelitis and pustulosis palmoplantarisB Björkstén, K H Gustavson, B Eriksson, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Hyperkalemic periodic paralysis caused by recurring mutation in the adult muscle sodium channel alpha-subunit geneA Sillén, C Wadelius, M Sundvall, et al.
Cancer Genetics and Cytogenetics|May 1, 1990
Benign ovarian teratomas. An analysis of their cellular originN Dahl, K H Gustavson, C Rune, et al.
Clinical Genetics|September 1, 1984
Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variationsG Annerén, B Arvidson, K H Gustavson, et al.
Acta Paediatrica Scandinavica|November 1, 1985
Selenium supplementation in X-linked muscular dystrophy. Effects on erythrocyte and serum selenium and on erythrocyte glutathione peroxidase activityM Gebre-Medhin, K H Gustavson, I Gamstorp, et al.
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