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- 95189571 contributor B7611403.
- 95189571 contributor B7611404.
- 95189571 created "1993.".
- 95189571 date "1993".
- 95189571 date "1993.".
- 95189571 dateCopyrighted "1993.".
- 95189571 description "Genotype-phenotype relationship -- Mutation rates in humans -- Direct and indirect analysis of human genetic disease -- Single base-pair substitution database -- Deletion database -- Examples of splice site mutations -- Amino acid symbols and the genetic code.".
- 95189571 description "Historical view of research into the nature of mutation -- Introduction to the structure, function and expression of human genes -- Human genetic disease, its analysis and diagnosis: an overview -- Methodology of mutation detection -- Indirect analysis of human genetic disease -- Single base-pair substitutions -- Gene deletions -- Gene insertions, duplications and inversions -- Single base-pair substitutions in human gene mRNA splice junctions and their phenotypic consequences -- Regulatory mutations -- Mutations affecting RNA processing and translation.".
- 95189571 description "Includes bibliographical references and index.".
- 95189571 extent "xiv, 402 p. :".
- 95189571 identifier "1872748414".
- 95189571 isPartOf "Human molecular genetics series.".
- 95189571 isPartOf "Human molecular genetics".
- 95189571 issued "1993".
- 95189571 issued "1993.".
- 95189571 language "eng".
- 95189571 publisher "Oxford, UK : Bios Scientific Publishers,".
- 95189571 subject "616/.042 21".
- 95189571 subject "Hereditary Diseases genetics.".
- 95189571 subject "Human genetics.".
- 95189571 subject "Humans Genetic disorders".
- 95189571 subject "QH431 .C716 1993".
- 95189571 tableOfContents "Genotype-phenotype relationship -- Mutation rates in humans -- Direct and indirect analysis of human genetic disease -- Single base-pair substitution database -- Deletion database -- Examples of splice site mutations -- Amino acid symbols and the genetic code.".
- 95189571 tableOfContents "Historical view of research into the nature of mutation -- Introduction to the structure, function and expression of human genes -- Human genetic disease, its analysis and diagnosis: an overview -- Methodology of mutation detection -- Indirect analysis of human genetic disease -- Single base-pair substitutions -- Gene deletions -- Gene insertions, duplications and inversions -- Single base-pair substitutions in human gene mRNA splice junctions and their phenotypic consequences -- Regulatory mutations -- Mutations affecting RNA processing and translation.".
- 95189571 title "Human gene mutation / David N. Cooper, Michael Krawczak.".
- 95189571 type "text".