Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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11 |
Material Type: Artigo
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Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndromeNicholls, R D ; Knoll, J H ; Butler, M G ; Karam, S ; Lalande, MNature (London), 1989-11, Vol.342 (6247), p.281-281 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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12 |
Material Type: Artigo
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Detection of Polymorphisms of Human DNA by Gel Electrophoresis as Single-Strand Conformation PolymorphismsOrita, Masato ; Iwahana, Hiroyuki ; Kanazawa, Hiroshi ; Hayashi, Kenshi ; Sekiya, TakaoProceedings of the National Academy of Sciences - PNAS, 1989-04, Vol.86 (8), p.2766-2770 [Periódico revisado por pares]Washington, DC: National Academy of Sciences of the United States of AmericaTexto completo disponível |
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13 |
Material Type: Artigo
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Robust Statistical Modeling Using the t DistributionLange, Kenneth L. ; Little, Roderick J. A. ; Taylor, Jeremy M. G.Journal of the American Statistical Association, 1989-12, Vol.84 (408), p.881-896 [Periódico revisado por pares]Alexandria, VA: Taylor & Francis GroupTexto completo disponível |
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14 |
Material Type: Artigo
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Association within a family of a balanced autosomal translocation with major mental illnessSt Clair, D. ; Blackwood, D. ; Muir, W. ; Walker, M. ; St Clair, D. ; Muir, W. ; Carothers, A. ; Spowart, G. ; Gosden, C. ; Evans, H.J.The Lancet (British edition), 1990-07, Vol.336 (8706), p.13-16 [Periódico revisado por pares]London: Elsevier LtdTexto completo disponível |
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15 |
Material Type: Artigo
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Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic NeuropathyWallace, Douglas C. ; Singh, Gurparkash ; Lott, Marie T. ; Hodge, Judy A. ; Schurr, Theodore G. ; Angela M. S. Lezza ; Elsas, Louis J. ; Nikoskelainen, Eeva K.Science (American Association for the Advancement of Science), 1988-12, Vol.242 (4884), p.1427-1430 [Periódico revisado por pares]Washington, DC: The American Association for the Advancement of ScienceTexto completo disponível |
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16 |
Material Type: Artigo
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Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemiaInnerarity, TL ; Mahley, RW ; Weisgraber, KH ; Bersot, TP ; Krauss, RM ; Vega, GL ; Grundy, SM ; Friedl, W ; Davignon, J ; McCarthy, BJJournal of lipid research, 1990-08, Vol.31 (8), p.1337-1349 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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17 |
Material Type: Artigo
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A new mitochondrial disease associated with mitochondrial DNA heteroplasmyHOLT, I. J ; HARDING, A. E ; PETTY, R. K. H ; MORGAN-HUGHES, J. AAmerican journal of human genetics, 1990-03, Vol.46 (3), p.428-433 [Periódico revisado por pares]Chicago, IL: University of Chicago PressTexto completo disponível |
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18 |
Material Type: Artigo
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A point mutation of the rhodopsin gene in one form of retinitis pigmentosaDryja, Thaddeus P ; McGee, Terri L ; Reichel, Elias ; Hahn, Lauri B ; Cowley, Glenn S ; Yandell, David W ; Sandberg, Michael A ; Berson, Eliot LNature (London), 1990-01, Vol.343 (6256), p.364-366 [Periódico revisado por pares]London: Nature PublishingTexto completo disponível |
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19 |
Material Type: Artigo
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Identification of Mutations in the COL4A5 Collagen Gene in Alport SyndromeBarker, David F. ; Hostikka, Sirkka Liisa ; Zhou, Jing ; Chow, Louise T. ; Oliphant, Arnold R. ; Gerken, Steven C. ; Gregory, Martin C. ; Skolnick, Mark H. ; Atkin, Curtis L. ; Tryggvason, KarlScience (American Association for the Advancement of Science), 1990-06, Vol.248 (4960), p.1224-1227 [Periódico revisado por pares]Washington, DC: American Society for the Advancement of ScienceTexto completo disponível |
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20 |
Material Type: Artigo
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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndromeHsiao, Karen ; Baker, Harry F ; Crow, Tim J ; Poulter, Mark ; Owen, Frank ; Terwilliger, Joseph D ; Westaway, David ; Ott, Jurg ; Prusiner, Stanley BNature (London), 1989-03, Vol.338 (6213), p.342-345 [Periódico revisado por pares]London: Nature PublishingTexto completo disponível |