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Clinical Genetics|October 1, 1988
Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish familyM Anvret, C Gillberg, J Wahlström, et al.Human Genetics|March 1, 1991
Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomereM Anvret, M Nordenskjöld, L Stolpe, et al.Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Achondroplasia in Sweden caused by the G1138A mutation in FGFR3A Alderborn, M Anvret, K H Gustavson, et al.Annals of Neurology|September 11, 1999
Genetic linkage of Welander distal myopathy to chromosome 2p13G Ahlberg, D von Tell, K Borg, et al.Genomics|May 1, 1994
Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish originZ P Zhang, M Blombäck, N Egberg, et al.Brain & Development|January 1, 1990
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte cultureJ Wahlström, I Witt-Engerström, L Mellquist, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Alcohol dehydrogenase alleles in Parkinson's diseaseS Buervenich, O Sydow, A Carmine, et al.Clinical Genetics|January 1, 1993
Hemophilia B in a 46,XX female probably caused by non-random X inactivationC Wadelius, M Lindstedt, M Pigg, et al.Human Molecular Genetics|September 1, 1993
Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophyM Anvret, G Ahlberg, U Grandell, et al.American Journal of Medical Genetics|January 1, 1991
Aicardi syndrome: early neuroradiological manifestations and results of DNA studies in one patientK B Nielsen, M Anvret, O Flodmark, et al.Pageof 18