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Human Molecular Genetics|May 1, 1997
Reduced penetrance of the Huntington's disease mutationS M McNeil, A Novelletto, J Srinidhi, et al.Human Molecular Genetics|September 1, 1995
Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrumE P Leeflang, L Zhang, S Tavaré, et al.Blood|October 1, 1984
Chromosome-mediated transfer of the malignant phenotype by human acute myelogenous leukemic cellsM D Minden, J F Gusella, D HousmanJournal of Medical Genetics|July 31, 2007
Factors associated with HD CAG repeat instability in Huntington diseaseV C Wheeler, F Persichetti, S M McNeil, et al.The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|May 1, 1997
Heterogeneous topographic and cellular distribution of huntingtin expression in the normal human neostriatumR J Ferrante, C A Gutekunst, F Persichetti, et al.Somatic Cell and Molecular Genetics|September 1, 1991
New DNA markers in the Huntington's disease gene candidate regionC S Lin, M Altherr, G Bates, et al.Somatic Cell and Molecular Genetics|January 1, 1993
A genetic linkage map of the chromosome 4 short armP A Locke, M E MacDonald, J Srinidhi, et al.Molecular Biology & Medicine|February 1, 1991
Molecular pathology of gyrate atrophy of the choroid and retina due to ornithine aminotransferase deficiencyV Ramesh, J F Gusella, V E ShihBrain Pathology (Zurich, Switzerland)|April 1, 1995
Neuropathology and molecular genetics of neurofibromatosis 2 and related tumorsD N Louis, V Ramesh, J F GusellaCancer Surveys|January 1, 1990
Progress towards the isolation and characterization of the genes causing neurofibromatosisA G Menon, J F Gusella, B R SeizingerPageof 29