检索结果 - Smith, D I

Isolation and mapping of a polymorphic DNA sequence (cA476) on chromosome 3 [D3S94] 由 Kiousis, S, Drabkin, H, Smith, D I

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Identification of two cosmids derived from within chromosomal band 3p21.1 that contain clusters of rare restriction sites and evolutionarily conserved sequences. 由 Smith, D I, Golembieski, W, Drabkin, H, Kiousis, S

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Isolation and mapping of a polymorphic sequence (3UCI 10) on chromosome 3 [D3S8]. 由 Smith, D I, Kiousis, S, Drabkin, H, Wasmuth, J

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The isolation and partial characterization of a new restriction endonuclease from Providencia stuartii. 由 Smith, D I, Blattner, F R, Davies, J

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Isolation and mapping of a polymorphic DNA sequence (lambda 64) on chromosome 3 [D3S95] 由 Smith, D I, Kiousis, S, Miller, D, Aleixandre, C, Wasmuth, J

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A cloned major Schistosoma mansoni egg antigen with homologies to small heat shock proteins elicits Th1 responsiveness. 由 Cai, Y, Langley, J G, Smith, D I, Boros, D L

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Effects of chronic fluoxetine treatment in the presence and absence of (±)pindolol: a microdialysis study 由 Dawson, L A, Nguyen, H Q, Smith, D I, Schechter, L E

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Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations. 由 Liu, W, Smith, D I, Rechtzigel, K J, Thibodeau, S N, James, C D

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Overabundance of rare-cutting restriction endonuclease sites in the human genome. 由 Smith, D I, Golembieski, W, Gilbert, J D, Kizyma, L, Miller, O J

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The human loci DNF15S2 and D3S94 have a high degree of sequence similarity to acyl-peptide hydrolase and are located at 3p21.3. 由 Ginzinger, D G, Shridhar, V, Baldini, A, Taggart, R T, Miller, O J, Smith, D I

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Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel. 由 Gerber, M J, Drabkin, H A, Firnhaber, C, Miller, Y E, Scoggin, C H, Smith, D I

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Isolation of large numbers of chromosome 3-specific cosmids containing clusters of rare restriction-endonuclease sites. 由 Golembieski, W A, Smith, S E, Recchia, F, Judge, A, Shridhar, V, Miller, O J, Drabkin, H, Smith, D I

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Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome. 由 Drumheller, T, McGillivray, B C, Behrner, D, MacLeod, P, McFadden, D E, Roberson, J, Venditti, C, Chorney, K, Chorney, M, Smith, D I

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Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease. 由 Seizinger, B R, Smith, D I, Filling-Katz, M R, Neumann, H, Green, J S, Choyke, P L, Anderson, K M, Freiman, R N, Klauck, S M, Whaley, J

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A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apart. 由 Secore, S L, Walker, A P, Herbstreith, M H, Siddique, T, Jeffers, A J, DeShields, T R, Speer, M C, Pericak-Vance, M A, Golembieski, W A, Smith, D I

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Differential screening of a human chromosome 3 library identifies hepatocyte growth factor-like/macrophage-stimulating protein and its receptor in injured lung. Possible implicatio... 由 Willett, C G, Smith, D I, Shridhar, V, Wang, M H, Emanuel, R L, Patidar, K, Graham, S A, Zhang, F, Hatch, V, Sugarbaker, D J, Sunday, M E

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Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26. 由 Pericak-Vance, M A, Nunes, K J, Whisenant, E, Loeb, D B, Small, K W, Stajich, J M, Rimmler, J B, Yamaoka, L H, Smith, D I, Drabkin, H A

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