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Prenatal Diagnosis|March 1, 1996
Prenatal diagnosis of X-linked myotubular myopathy: strategies using new and tightly linked DNA markersL J Hu, J Laporte, W Kress, et al.Genomics|November 1, 1988
Tight linkage between type III Gaucher's disease (Norrbottnian type) and a MspI polymorphism within the gene for human glucocerebrosidaseN Dahl, A Erikson, K Hammarström-Heeroma, et al.Acta Ophthalmologica Scandinavica|January 9, 1999
Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian familiesH Arnell, M Mäntyjärvi, K Tuppurainen, et al.Human Genetics|March 1, 1988
DNA linkage analysis of X-linked retinoschisisN Dahl, P Goonewardena, J Chotai, et al.Frontiers in Cell and Developmental Biology|November 20, 2018
The Emerging Role of Lamin C as an Important <i>LMNA</i> Isoform in MechanophenotypeRafael D González-Cruz, Kris N Dahl, Eric M DarlingClinical Genetics|August 18, 1999
A microdeletion syndrome due to a 3-Mb deletion on 19q13.2--Diamond-Blackfan anemia associated with macrocephaly, hypotonia, and psychomotor retardationH Cario, H Bode, P Gustavsson, et al.Journal of Clinical Neuromuscular Disease|December 17, 2008
Charcot-marie-tooth disease with cerebellar atrophyA Melberg, R Raininko, N Dahl, et al.Cancer Research|September 1, 1976
Inhibitory and cytotoxic effects of Oncovin (Vincristine sulfate) on cells of human line NHIK 3025W N Dahl, R Oftebro, E O Pettersen, et al.American Journal of Human Genetics|January 1, 1990
Mapping of the gene for X-linked amelogenesis imperfecta by linkage analysisM Lagerström, N Dahl, L Iselius, 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.Pageof 14