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Clinical Genetics|November 1, 1996
Glycerol kinase deficiency in two brothers with and without clinical manifestationsH K Blomquist, N Dahl, L Gustafsson, et al.Clinical Genetics|July 8, 2017
Homozygosity for a missense variant in COMP gene associated with severe pseudoachondroplasiaM Tariq, T N Khan, L Lundin, et al.IJTLD Open|January 19, 2026
Treatment and outcomes in patients with non-TB mycobacterial pulmonary disease: a single-centre studyV N Dahl, A Fløe, F Rudolf, et al.American Journal of Human Genetics|August 1, 1989
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304)N Dahl, P Goonewardena, H Malmgren, et al.European Journal of Human Genetics : EJHG|August 10, 1999
Deletion including the oligophrenin-1 gene associated with enlarged cerebral ventricles, cerebellar hypoplasia, seizures and ataxiaD Tentler, P Gustavsson, J Leisti, et al.American Journal of Human Genetics|June 1, 1993
Linkage mapping of a severe X-linked mental retardation syndromeH Malmgren, M Sundvall, N Dahl, et al.Transplantation Proceedings|September 30, 2023
The Diagnostic Yield and Clinical Impact of Systematic Screening of Kidney Transplant Candidates by Cardiac Computed Tomography: A Cohort StudyMarie B Nielsen, Malene S Iversen, Amal Derai, et al.Muscle & Nerve|December 1, 1996
Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadismA Melberg, H Arnell, N Dahl, et al.American Journal of Medical Genetics|January 23, 2002
A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpointD Tentler, G Brandberg, C Betancur, et al.Journal of the Neurological Sciences|December 1, 1995
Autosomal dominant cerebellar ataxia deafness and narcolepsyA Melberg, J Hetta, N Dahl, et al.Pageof 14