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American Journal of Human Genetics|May 1, 1995
Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb regionN Dahl, L J Hu, M Chery, et al.
American Journal of Medical Genetics|February 1, 1991
Multipoint linkage analysis of DXS369 and DXS304 in fragile X familiesB A van Oost, A Smits, J C Dreesen, et al.
Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.
American Journal of Human Genetics|May 1, 1997
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancerS Håkansson, O Johannsson, U Johansson, et al.
American Journal of Medical Genetics|February 1, 1991
Mapping of a cerebellar degeneration related protein and DXS304 around the fragile siteM C Hirst, M V Bell, R N MacKinnon, et al.
Journal of Cardiovascular Computed Tomography|January 19, 2024
Optimal diagnostic approach for using CT-derived quantitative flow ratio in patients with stenosis on coronary computed tomography angiographyJonathan N Dahl, Laust D Rasmussen, Daixin Ding, et al.
Annals of Neurology|September 2, 2000
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10qA Melberg, A Oldfors, C Blomström-Lundqvist, et al.
American Journal of Human Genetics|June 1, 1996
Mutations and phenotype in isolated glycerol kinase deficiencyA P Walker, F Muscatelli, A N Stafford, et al.
Open Forum Infectious Diseases|November 11, 2025
Mortality and Causes of Death in Patients With <i>Mycobacterium avium</i> Complex Isolates Through 28 YearsVictor N Dahl, Andreas A Pedersen, Isik S Johansen, et al.
Blood Cells, Molecules & Diseases|February 7, 2006
Erythropoiesis in the Rps19 disrupted mouse: Analysis of erythropoietin response and biochemical markers for Diamond-Blackfan anemiaH Matsson, E J Davey, A S Fröjmark, et al.
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