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" The Human Genome Project and its impact on the study of human disease. "
Thompson & Thompson, Genética en medicina, 5a ed. ©2004 Últ. Reimpr. 2005 - Página 139
por Margaret W. Thompson, Robert L. Nussbaum, Roderick R. McInnes, Huntington F. Willard - 2004 - 584 páginas
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Biochemistry of Exercise X, Volumen10

Mark Hargreaves - 1999 - 337 páginas
...FS Sequencing the human genome. Hasp. Pract. 32: 35-54; 1997. 5. Green, ED, Cox, DR, and Myers, RM The human genome project and its impact on the study of human disease. In The metabolic and molecular bases of inherited disease (Vol. 1; 7th Ed.). Ed. CR Scriver, AL Beaudet,...
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Color Atlas of Genetics

Eberhard Passarge - 2001 - 457 páginas
...References Brown, TA: Genomes. Bios Scientific Publishers, Oxford, 1999. Green, ED. Cox. DR Myers. RM: The human genome project and its impact on the study of human disease, pp. 401 -436. In: Scriver. CR. et al., eds. The Metabolic and Molecular Bases of Inherited Disease....
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Responsible Conduct of Research

Adil E. Shamoo, David B. Resnik - 2003 - 345 páginas
...Graham, G., 1999. The Internet: A Philosophical Inquiry. Routledge, London. "Green, ED, et al., 1995. The Human Genome Project and Its Impact on the Study of Human Beings. In The Metaholic and Molecular Basis of Inherited Disease. Scriver et al. (eds.), pp. 401-55....
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Nutrigenetics and Nutrigenomics

Artemis P. Simopoulos, J. M. Ordovas - 2004 - 324 páginas
...Wolf B: Disorders of biotin metabolism; in Scriver C, Beaudet AL, Sly WS, Vogelstein B, Kinzler KW, Valle D, et al (eds): The Metabolic and Molecular Bases of Inherited Disease, ed 8. New York, McGraw-Hill, 2001, pp 3935-3962. 30 Singh IN, Dakshinamurti K: Stimulation...
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Molecular Mechanisms of Atherosclerosis

Joseph Loscalzo - 2004 - 312 páginas
...role of apolipoprotein E in normal and abnormal lipoprotein metabolism. In: Scriver CR, Beaudet AL, Valle D et al, eds. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill, 2001:2835-2862. 8. Fredrickson DS, Lees RS. Familial hyperlipoproteinemia....
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Marks' Essential Medical Biochemistry

Michael Lieberman, Allan D. Marks, Colleen M. Smith, Dawn B. Marks - 2007 - 565 páginas
...abnormalities. Suggested References • Brusilow S, Horwich A. Urea cycle enzymes. In: Scriver CR, Beaudet AL, Valle D, et al., eds. The Metabolic and Molecular Bases of Inherited Disease, vol II. 8th ed. New York: McGraw-Hill. 2001:1909-1963. • Marshall E. Gene therapy death...
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Molecular Pathology in Clinical Practice

Debra G.B. Leonard - 2007 - 600 páginas
...sequence. (Reprinted with permission from Sadler AJE. Von Willebrand disease. In: Scriver CR, Beaudet AL, Valle D, et al., eds. The Metabolic and Molecular Bases of Inherited Disease. Copyright 2001 McGraw-Hill.) Signal peptide Propeptide VWF 1 23 763 2813 V D1 D2 D' D3 A1...
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Primary Immunodeficiency Diseases: A Molecular & Cellular Approach

Hans D. Ochs, C. I. Edward Smith, Jennifer M. Puck - 2006 - 776 páginas
...deficiency in two patients with severely impaired cellular immunity. Lancet 2: 1067-1069, 1972. Green ED. The Human Genome Project and its impact on the study...disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Bases of Inherited Disease, 8th ed. New York: McGraw-Hill, pp. 259-298,...
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