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Proceedings of the National Academy of Sciences of the United States of America|March 1, 1993
Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer diseaseW J Strittmatter, A M Saunders, D Schmechel, et al.Neurogenetics|March 25, 2000
Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) geneJ R Gilbert, V Guy, A Kumar, et al.Proceedings of the National Academy of Sciences of the United States of America|November 14, 1997
Transglutaminase-catalyzed inactivation of glyceraldehyde 3-phosphate dehydrogenase and alpha-ketoglutarate dehydrogenase complex by polyglutamine domains of pathological lengthA J Cooper, K R Sheu, J R Burke, et al.Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
DNA linkage analysis of X chromosome-linked chronic granulomatous diseaseR L Baehner, L M Kunkel, A P Monaco, et al.Archives of Neurology|June 1, 1996
Motor changes in presymptomatic Huntington disease gene carriersE Siemers, T Foroud, D J Bill, et al.Neurology|March 12, 2003
Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson diseaseT Foroud, S K Uniacke, L Liu, et al.Genomics|January 1, 1989
A genetic linkage map of the long arm of human chromosome 22G A Rouleau, J L Haines, A Bazanowski, et al.Cellular and Molecular Life Sciences : CMLS|September 25, 2003
Pharmacogenetics and disease genetics of complex diseasesV D Schmith, D A Campbell, S Sehgal, et al.Clinical Genetics|June 1, 1989
Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometryN G Laing, T Siddique, R Bartlett, et al.Neurology|April 1, 1990
Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studiesM C Speer, M A Pericak-Vance, L Yamaoka, et al.Pageof 37