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Results: 1-25 | 26-31 |
Results: 26-31/31
An autosomal genomic screen for autism
Authors: Barrett, S Beck, JC Bernier, R Bisson, E Braun, TA Casavant, TL Childress, D Folstein, SE Garcia, M Gardiner, MB Gilman, S Haines, JL Hopkins, K Landa, R Meyer, NH Mullane, JA Nishimura, DY Palmer, P Piven, J Purdy, J Santangelo, SL Searby, C Sheffield, V Singleton, J Slager, S Struchen, T Svenson, S Vieland, V Wang, K Winklosky, B
Citation: S. Barrett et al., An autosomal genomic screen for autism, AM J MED G, 88(6), 1999, pp. 609-615
Further evidence linking late-onset Alzheimer disease with chromosome 12
Authors: Scott, WK Grubber, JM Abou-Donia, SM Church, TD Saunders, AM Roses, AD Pericak-Vance, MA Conneally, PM Small, GW Haines, JL
Citation: Wk. Scott et al., Further evidence linking late-onset Alzheimer disease with chromosome 12, J AM MED A, 281(6), 1999, pp. 513-514
Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22
Authors: Bejaoui, K McKenna-Yasek, D Hosler, BA Burns-Deater, E Deater, LM O'Neill, G Haines, JL Brown, RH
Citation: K. Bejaoui et al., Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22, NEUROLOGY, 52(3), 1999, pp. 510-515
Memory self-appraisal in middle-aged and older adults with the apolipoprotein e-4 allele
Authors: Small, GW Chen, ST Komo, S Ercoli, L Bookheimer, S Miller, K Lavretsky, H Saxena, S Kaplan, A Dorsey, D Scott, WK Saunders, AM Haines, JL Roses, AD Pericak-Vance, MA
Citation: Gw. Small et al., Memory self-appraisal in middle-aged and older adults with the apolipoprotein e-4 allele, AM J PSYCHI, 156(7), 1999, pp. 1035-1038
Association of COL1A1 and otosclerosis - Evidence for a shared genetic etiology with mild osteogenesis imperfecta
Authors: McKenna, MJ Kristiansen, AG Bartley, ML Rogus, JJ Haines, JL
Citation: Mj. Mckenna et al., Association of COL1A1 and otosclerosis - Evidence for a shared genetic etiology with mild osteogenesis imperfecta, AM J OTOL, 19(5), 1998, pp. 604-610
Comprehensive mutational analysis of the TSC1 gene: observations on frequency of mutation, associated features, and nonpenetrance
Authors: Kwiatkowska, J Jozwiak, S Hall, F Henske, EP Haines, JL McNamara, P Braiser, J Wigowska-Sowinska, J Kasprzyk-Obara, J Short, MP Kwiatkowski, DJ
Citation: J. Kwiatkowska et al., Comprehensive mutational analysis of the TSC1 gene: observations on frequency of mutation, associated features, and nonpenetrance, ANN HUM GEN, 62, 1998, pp. 277-285
Risultati: 1-25 | 26-31 |