Matches in Harvard for { <http://id.lib.harvard.edu/aleph/003990365/catalog> ?p ?o. }
Showing items 1 to 33 of
33
with 100 items per page.
- catalog contributor b5745235.
- catalog created "c1994.".
- catalog date "1994".
- catalog date "c1994.".
- catalog dateCopyrighted "c1994.".
- catalog description "(cont) Use of DNA polymorphisms in predicting genetic risks -- Single markers in familial cases -- Flanking markers in familial cases -- Single markers and potentially new mutations -- Flanking markers and potentially new mutations -- Direct detection of mutations -- Uniparental disomy -- Genetic heterogeneity -- Linkage disequilibrium and haplotype analysis -- When do mutations occur? -- Integration of RFLP data with non-DNA parameters -- Biochemical test results -- Incomplete penetrance and age-at-onset corrections -- Decoding lod scores -- Pascal's triangle and the binomial expansion -- Program to generate phase values for flanking markers and reduced penetrance or delayed age at onset.".
- catalog description "General introduction to the estimation of genetic risks -- Mendelian risk -- Risk modified by reproductive history -- Risk based upon phenotype -- Risk based upon genotype -- Familial versus new mutations -- Meiotic versus mitotic mutations -- Non-Mendelian genetic mechanisms -- Bayesian risk calculations for X-linked recessive disorders -- Unaffected sons -- Daughters with unaffected grandsons -- Which branches of the family may be used? -- Negative family history -- Incorporation of females with biochemical test results into bayesian calculations -- Linearity of the test results -- Column ratios -- Biochemical tests on the consultand herself -- Stating conditional probabilities in words -- Resolution of conflicting evidence -- Noncarrier ratios -- Negative family history -- Pedigree risks in autosomal conditions -- Autosomal dominant inheritance -- Autosomal recessive inheritance -- Introduction to DNA polymorphisms -- Statistical approaches to gene mapping -- Iod scores -- Probabilities over pedigrees -- Multipoint linkage analysis.".
- catalog description "Includes bibliographical references and index.".
- catalog extent "xviii, 195 p. :".
- catalog hasFormat "Calculation of genetic risks.".
- catalog identifier "0801846781 (hc : alk. paper)".
- catalog isFormatOf "Calculation of genetic risks.".
- catalog issued "1994".
- catalog issued "c1994.".
- catalog language "eng".
- catalog publisher "Baltimore : Johns Hopkins University Press,".
- catalog relation "Calculation of genetic risks.".
- catalog subject "616/.042 20".
- catalog subject "DNA Probes diagnostic use.".
- catalog subject "Genetic Diseases, Inborn epidemiology.".
- catalog subject "Genetic Diseases, Inborn genetics.".
- catalog subject "Genetic disorders Diagnosis.".
- catalog subject "Genetic disorders Risk factors.".
- catalog subject "Health risk assessment.".
- catalog subject "Molecular Probe Techniques.".
- catalog subject "QZ 50 B851c 1994".
- catalog subject "RB155.6 .B75 1994".
- catalog subject "Risk Factors.".
- catalog subject "Risk factors.".
- catalog tableOfContents "(cont) Use of DNA polymorphisms in predicting genetic risks -- Single markers in familial cases -- Flanking markers in familial cases -- Single markers and potentially new mutations -- Flanking markers and potentially new mutations -- Direct detection of mutations -- Uniparental disomy -- Genetic heterogeneity -- Linkage disequilibrium and haplotype analysis -- When do mutations occur? -- Integration of RFLP data with non-DNA parameters -- Biochemical test results -- Incomplete penetrance and age-at-onset corrections -- Decoding lod scores -- Pascal's triangle and the binomial expansion -- Program to generate phase values for flanking markers and reduced penetrance or delayed age at onset.".
- catalog tableOfContents "General introduction to the estimation of genetic risks -- Mendelian risk -- Risk modified by reproductive history -- Risk based upon phenotype -- Risk based upon genotype -- Familial versus new mutations -- Meiotic versus mitotic mutations -- Non-Mendelian genetic mechanisms -- Bayesian risk calculations for X-linked recessive disorders -- Unaffected sons -- Daughters with unaffected grandsons -- Which branches of the family may be used? -- Negative family history -- Incorporation of females with biochemical test results into bayesian calculations -- Linearity of the test results -- Column ratios -- Biochemical tests on the consultand herself -- Stating conditional probabilities in words -- Resolution of conflicting evidence -- Noncarrier ratios -- Negative family history -- Pedigree risks in autosomal conditions -- Autosomal dominant inheritance -- Autosomal recessive inheritance -- Introduction to DNA polymorphisms -- Statistical approaches to gene mapping -- Iod scores -- Probabilities over pedigrees -- Multipoint linkage analysis.".
- catalog title "The calculation of genetic risks : worked examples in DNA diagnostics / Peter J. Bridge.".
- catalog type "text".