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European Journal of Cancer & Clinical Oncology|October 1, 1983
Epstein-Barr virus markers in a series of Burkitt's lymphomas from the West Nile District, UgandaA Geser, G M Lenoir, M Anvret, et al.British Medical Journal (Clinical Research Ed.)|February 7, 1981
Epstein-Barr-virus-carrying lymphoma in a patient with ataxia-telangiectasiaA K Saemundsen, A I Berkel, W Henle, et al.The New England Journal of Medicine|February 18, 1993
Direct diagnosis of myotonic dystrophy with a disease-specific DNA markerP Shelbourne, J Davies, J Buxton, et al.Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.Antisense & Nucleic Acid Drug Development|January 26, 1999
Failure to achieve gene conversion with chimeric circular oligonucleotides: potentially misleading PCR artifacts observedZ Zhang, M Eriksson, G Falk, et al.Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1997
Treatment of adrenoleukodystrophy with bone marrow transplantationG Malm, O Ringdén, M Anvret, et al.American Journal of Human Genetics|June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusK Johnson, P Shelbourne, J Davies, et al.American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.Human Genetics|January 1, 1993
X chromosome linkage studies in familial Rett syndromeA R Curtis, S Headland, S Lindsay, et al.Pageof 18