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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.Journal of Medical Genetics|February 9, 2000
A microdeletion in 19q13.2 associated with mental retardation, skeletal malformations, and Diamond-Blackfan anaemia suggests a novel contiguous gene syndromeD Tentler, P Gustavsson, G Elinder, et al.American Journal of Medical Genetics|March 1, 1993
New X-linked syndrome with severe mental retardation, severely impaired vision, severe hearing defect, epileptic seizures, spasticity, restricted joint mobility, and early deathK H Gustavson, G Annerén, H Malmgren, et al.European Journal of Human Genetics : EJHG|January 15, 1999
Strong founder effect for a transglutaminase 1 gene mutation in lamellar ichthyosis and congenital ichthyosiform erythroderma from NorwayM Pigg, T Gedde-Dahl, D Cox, et al.Genomics|August 1, 1991
A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)M Lagerström, N Dahl, Y Nakahori, et al.European Journal of Medical Genetics|May 14, 2013
Cenani-Lenz syndrome restricted to limb and kidney anomalies associated with a novel LRP4 missense mutationTahir Naeem Khan, J Klar, Zafar Ali, et al.Journal of Medical Genetics|October 10, 1997
Diamond-Blackfan anaemia in a girl with a de novo balanced reciprocal X;19 translocationP Gustavsson, G Skeppner, B Johansson, et al.Experimental Hematology|January 11, 1992
Circulating macrophage colony-stimulating factor is not reduced in malignant osteopetrosisP J Orchard, N Dahl, S L Aukerman, et al.American Journal of Medical Genetics|February 1, 1991
Molecular characterization of a DNA probe, U6.2, located close to the fragile X locusR Pergolizzi, W T Brown, P Goonewardena, et al.Neurology|December 22, 1999
Neuroimaging study in autosomal dominant cerebellar ataxia, deafness, and narcolepsyA Melberg, N Dahl, J Hetta, et al.Pageof 14