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Human Molecular Genetics|June 1, 1993
Mouse neurofibromatosis type 1 cDNA sequence reveals high degree of conservation of both coding and non-coding mRNA segmentsA Bernards, A J Snijders, G E Hannigan, et al.Human Mutation|January 1, 1992
A 15-bp deletion in exon 5 of the ornithine aminotransferase (OAT) locus associated with gyrate atrophyJ K Park, J J O'Donnell, V E Shih, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1992
The alpha-subunit of the skeletal muscle sodium channel is encoded proximal to Tk-1 on mouse chromosome 11C Ambrose, S Cheng, B Fontaine, et al.Developmental Neuroscience|January 1, 1987
Models for inherited susceptibility to cancer in the nervous system: a molecular-genetic approach to neurofibromatosisB R Seizinger, R L Martuza, G Rouleau, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1988
Mapping of the gene encoding the beta-amyloid precursor protein and its relationship to the Down syndrome region of chromosome 21D Patterson, K Gardiner, F T Kao, et al.Genomics|September 1, 1993
A high-resolution linkage map of human 9q34.1E P Henske, L Ozelius, J F Gusella, et al.Annals of Neurology|February 1, 1991
Loss of chromosome 22 alleles in human sporadic spinal schwannomasB Fontaine, M P Hanson, J P VonSattel, et al.Human Molecular Genetics|March 4, 2000
Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in HdhQ92 and HdhQ111 knock-in miceV C Wheeler, J K White, C A Gutekunst, et al.DNA (Mary Ann Liebert, Inc.)|December 1, 1986
Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferaseV Ramesh, M M Shaffer, J M Allaire, et al.Journal of Medical Genetics|February 1, 1990
Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locusI Kondo, H Ohta, M Yazaki, et al.Pageof 29