| Announcement |
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| Hereditary tumors, Brandi ML, White R (eds), Rome Italy: Serano Symposia Publications from Raven Press, V. 83,218 pp. $69.50, 1991 |
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| Estimation of the frequency of isoform–genotype discrepancies at the apolipoprotein E locus in heterozygotes for the isoforms |
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✓ |
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| Announcement |
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| Preliminary ordering of multiple linked loci using pairwise linkage data |
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| Molecular basis of a unique African Variant (A‐IV 5) of human apolipoprotein A‐IV and its significance in lipid metabolism |
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blacks; black allele |
| Longitudinal study of the association between ABO phenotype and total serum cholesterol level in a Japanese cohort |
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West European populations; nonwhite populations; various racial groups; Japanese |
| Effect of cohort differences in smoking prevalence on models of lung cancer susceptibility |
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| Masthead |
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| Two common polymorphisms in the APO A‐IV coding gene: Their evolution and linkage disequilibrium |
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| Segregation analysis of height‐adjusted weight with generation‐ and age‐dependent effects: The Nancy family study |
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| Masthead |
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| Pedigree analysis of blood pressure in subjects from rural Greece and relatives who migrated to Melbourne, Australia |
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| Dietary intake and gene variation influence the response of plasma lipids to dietary intervention |
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| Family study of α<sub>1</sub>‐antitrypsin deficiency: Effects of cigarette smoking, measured genotype, and their interaction on pulmonary function and biochemical traits |
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| Commingling analysis of memory performance in offspring of Alzheimer patients |
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| Two‐Locus models of disease |
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| Masthead |
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| Numerical comparisons of two formulations of the logistic regressive models with the mixed model in segregation analysis of discrete traits |
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| Elementary methods for the analysis of dichotomous outcomes in unselected samples of Twins |
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| Segregation analysis of 159 soft tissue sarcoma kindreds: Comparison of fixed and sequential sampling schemes |
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| Adequacy of single‐locus approximations for linkage analyses of oligogenic traits |
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| An analytical method for assessing patterns of familial aggregation in case‐control studies |
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| Masthead |
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| Familial analysis of eosinophilia caused by helminthic parasites |
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| Do bilineal pedigrees represent a problem for linkage analysis? basic principles and simulation results for single‐gene diseases with no heterogeneity |
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| Detection of linkage under heterogeneity: Comparison of the two‐locus vs. admixture models |
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| Genetic Epidemiology and genetic Epidemiology |
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| Linkage studies of schizophrenia: A simulation study of statistical power |
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| Detection of genetic heterogeneity for complex quantitative phenotypes |
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| Using multidimensional scaling on data from pairs of relatives to explore the dimensionality of categorical multifactorial traits |
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| Specificity and sensitivity of hexosaminidase assays and DNA analysis for the detection of tay‐sachs disease gene carriers among Ashkenazic Jews |
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✓ |
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Ashkenazic Jews; Ashkenazim |
| Apolipoprotein B‐gene DNA polymorphisms (X<i>ba</i>l and <i>Eco</i>RI), serum lipids, and apolipoproteins in healthy Chinese |
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✓ |
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Chinese |
| Genetic and environmental effects on blood pressure in a Norwegian sample |
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| Two‐locus mitochondrial and nuclear gene models for mitochondrial disorders |
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| Sensitivity of transmission probabilities to paternity exclusion in segregation analysis |
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| Masthead |
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| Extended pedigree patterned covariance matrix mixed models for quantitative phenotype analysis |
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| Apolipoprotein E polymorphism in a Danish population compared to findings in 45 other study populations around the world |
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northern regions of Europe; Asian |
| Genetic variation in two bone‐related proteins: Is there an association with bone mineral density or skeletal size in postmenopausal women? |
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non-Black |
| Masthead |
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| Genetic markers associated with high density lipoprotein cholesterol levels in a biracial population sample |
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✓ |
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