Showing results (1-10 of 134) with videos related to
Sort By:
Pageof 14
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1988
Use of linked DNA probes for carrier detection and diagnosis of X-linked juvenile retinoschisisN Dahl, U PetterssonLakartidningen|January 30, 1991
[The Norrbothnian type of Gaucher's disease. Mutation diagnosis as a simple technique for risk determination]N Dahl, A EriksonCalcified Tissue International|July 1, 1993
Malignant osteopetrosis: c-src kinase is not reduced in fibroblastsG Meyerson, N Dahl, S PåhlmanClinical Genetics|February 1, 1993
Intrafamilial variation in Leber hereditary optic neuropathy revealed by direct mutation analysisL Cavelier, U Gyllensten, N DahlActa Oto-Laryngologica|April 25, 2000
Audiometric characterization of a family with digenic autosomal, dominant, progressive sensorineural hearing lossE Borg, E Samuelsson, N DahlAnnual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 25, 2010
The nucleus as a central structure in defining the mechanical properties of stem cellsA S Ribeiro, K N DahlDiabete & Metabolisme|December 1, 1995
Age-dependent differences in insulin secretion and intracellular handling of insulin in isolated pancreatic islets of the ratL A Borg, N Dahl, I SwenneHuman Genetics|November 1, 1993
Gaucher disease (Norrbottnian type III): probable founders identified by genealogical and molecular studiesN Dahl, P O Hillborg, A OlofssonAmerican Journal of Human Genetics|August 1, 1990
Gaucher disease type III (Norrbottnian type) is caused by a single mutation in exon 10 of the glucocerebrosidase geneN Dahl, M Lagerström, A Erikson, et al.Pageof 14