| Analysis of human genetic linkage. Jurg Ott. Baltimore: The Johns Hopkins University Press, 1985, 238 pp, $35.00 |
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| Masthead |
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| Interaction of genetics and epidemiology in the literature |
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| Complex segregation analysis of low levels of plasma high‐density lipoprotein cholesterol in a sample of nuclear families in Jerusalem |
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| Erratum |
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| Masthead |
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| Genetic analysis workshop IV: The 11p data sets |
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| Multilocus linkage analysis of markers located on short arm of chromosome 11 |
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| Development of a map of chromosome 11p |
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| Linkage analysis and multi-point mapping of 11p markers |
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| Multipoint mapping: Determining the order of the β-globin, ADJ, insulin and C-HA-RAS-1 loci |
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| Genetic analysis workshop IV: Huntington disease linkage analysis, data description |
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| Genetic analysis workshop IV: Huntington disease linkage analysis summary |
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| Analysis of Huntington disease linkage to G8 |
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| Linkage probability and its approximate confidence interval under possible heterogeneity |
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| Genetic analysis workshop IV: Some clinical, pathological and etiological aspects of two HLA-related diseases |
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| Family analysis for IDDM - HLA. Comparison of the two-allele model versus the three-allele model |
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| Genetic analysis workshop IV: Summary of the multiple sclerosis workshop |
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| Conditional linkage analysis of multiple sclerosis data |
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| Combined segregation and linkage analysis of multiple sclerosis |
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| Masthead |
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| Familial resemblance of bone mass in adult women |
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| Studies on an isolated West Indies population: IV. Genetic study of hearing loss |
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✓ |
✓ |
French origin |
| Familial aggregation of cancer in Laredo, Texas: A generally low‐risk Mexican‐American population |
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✓ |
✓ |
Mexican-American; Utah Mormons |
| Human parotid proline‐rich proteins: Correlation of genetic polymorphisms to dental caries |
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| Symptom patterns and causes of somatization in men: II. Genetic and environmental independence from somatization in women |
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| Log‐linear model analysis of allelic associations |
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| Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region |
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| Evidence for linkage between Wilson disease and esterase D in three kindreds: Detection of linkage for an autosomal recessive disorder by the family study method |
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✓ |
✓ |
Israeli‐Arab, Druze |
| Masthead |
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| Genetic etiology of gastric carcinoma: I. Chronic atrophic gastritis |
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| Genetic epidemiology of Menkes disease |
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| Description of a large pedigree with an adverse lipoprotein cholesterol phenotype: The Bogalusa Heart Study |
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| Linkage analysis of Von Recklinghausen neurofibromatosis: Chromosomes 4 and 19 |
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| Estimation of linkage disequilibrium from conditional haplotype data: Application to β‐globin gene cluster in American blacks |
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✓ |
✓ |
American blacks |
| Multiple regression analysis of twin data obtained from selected samples |
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| Examination of heterogeneity in 200 Danish breast cancer pedigrees |
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| Linkage relationships among four 11p markers in the Utah dataset |
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| Multipoint analysis of chromosome 11p markers |
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| Determination of the order of loci on the short arm of chromosome 11 using two and three locus linkage analyses of pedigree and sib pair data |
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| Disequilibrium on human chromosome 11p |
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| Linkage analysis between Huntington disease and the G8 marker locus |
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| Effect of age-at-onset specifications on Huntington disease - G8 linkage analysis |
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| Linkage studies and prediction of risks for Huntington disease |
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| Genetic analysis workshop IV: Summary for coeliac disease |
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| A synergistic three allele model for the HLA-linked components of coeliac disease predisposition |
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| Genetic analysis workshop IV: Insulin dependent diabetes mellitus - summary |
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| Masthead |
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| Cancer and autoimmune disease in families with common variable immune deficiency |
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| Announcement |
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| Symptom patterns and causes of somatization in men: I. Differentiation of two discrete disorders |
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✓ |
✓ |
Swedish |
| An approach to the multivariate analysis of high‐density‐lipoprotein cholesterol in a large kindred: The Bogalusa Heart Study |
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| Announcements |
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| Two‐disease locus model: Sib pair method using information on both HLA and Gm |
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| Erratum |
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| Masthead |
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| Prevalence and associations of apolipoprotein A‐I linked DNA polymorphisms: Results from a population study |
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| Causes of death in huntington disease as reported on death certificates |
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| Relationship of prevalence of non‐insulin‐dependent diabetes mellitus to Amerindian admixture in the Mexican Americans of San Antonio, Texas |
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✓ |
✓ |
Amerindian; Anglo; Mexican Americans |
| Congenital anomalies in American Indians of British Columbia |
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✓ |
✓ |
American Indians; Indian; non-Indians |
| Announcement |
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| Segregation and linkage analysis of breast cancer in the Dutch and Utah families |
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✓ |
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Dutch |
| Critique of a published analysis of the Jacobsen data |
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| A log-linear model for binary pedigree data |
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| Linkage analysis of Dutch families at high risk for breast cancer |
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| Genetic analysis workshop IV: Summary of two-point and multipoint mapping of 11p |
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| Two-point versus multipoint linkage analysis: A statistical view |
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| A genetic map of human chromosome 11p |
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| Strategies for efficient linkage analysis: Example of Huntington's disease pedigrees |
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| Linkage analysis of G8 and Huntington's disease |
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| Report on genetic linkage analysis between Huntington's disease and the G8 DNA polymorphism |
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| The genetic epidemiology of coeliac disease |
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| Discrimination between genetic models for insulin dependent diabetes mellitus |
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| Testing the simple 3-allele model of inheritance of IDDM at the HLA-associated locus |
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| HLA haplotype sharing in IDDM affected sib pairs as a function of HLA DR genotype |
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| Differential HLA haplotype sharing conditional on proband genotype is likely a necessary consequence of all three allele heterogeneity models: A rebuttal |
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| The inheritance of pyloric stenosis explained by a multifactorial threshold model with sex dimorphism for liability |
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| Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis |
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| Announcement |
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| Family history of cancer related to cholesterol level in young adults |
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| Testing for developmental changes in gene expression on resemblance for quantitative traits in kinships of twins: Application to height, weight, and blood pressure |
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| Heterogeneity in multifactorial inheritance of plasma lipids and lipoproteins in ethnically diverse families in Jerusalem |
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✓ |
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parents' country of birth (Europe, Asia, North Africa, and Israel/mixed origin); European group |
| Announcement |
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| Masthead |
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| Cleft lip with or without cleft palate: Reanalysis of a three‐generation family study from England |
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| The recurrence risks for isolated cases with incompletely penetrant X‐linked conditions |
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| Analysis of the distribution of erythrocyte sodium lithium countertransport in a sample representative of the general population |
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| Announcement |
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| Reuel A. Stallones: In memoriam |
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| Multipoint linkage analysis of spinocerebellar ataxia and markers on chromosome 6 |
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| Etiological heterogeneity in Hodgkin's disease: HLA linked and unlinked determinants of susceptibility independent of histological concordance |
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| Segregation analysis of the Jacobsen data |
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| A nonparametric test of heterogeneity of family risk |
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| Linkage analysis of breast cancer among Utah and Dutch families using the sib-pair test |
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| A strategy for multipoint ordering: Example of the 11p markers |
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| Combined segregation and linkage analysis of coeliac disease |
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| HLA and IDDM predisposition: New aspects |
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| Family and population analysis of multiple sclerosis |
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| Segregation analysis of hereditary nonpolyposis colorectal cancer |
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| Three alleles for quantitative Lp(a) |
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| On analysis of path models by the multivariate normal model for pedigree analysis |
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| Testing for familial aggregation of a dichotomous trait |
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| Preface |
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| Acknowledgments |
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| Genetic analysis of human breast cancer: Literature review and description of family data in workshop |
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| Genetic analysis of human breast cancer: A synthesis of contributions to Gaw IV |
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| A note on the basis of regressive models for genetic analysis |
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| A scoring method for multi-point linkage analysis: Application to the Utah 11-p data |
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| Sex differences in recombination fraction estimates and their effect on ordering of chromosome 11 markers |
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| Analysis of Huntington disease linkage and age-of-onset distributions |
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| Ascertainment considerations in the analysis of affected sib shared haplotype data |
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| HLA-DR effects in a large German IDDM dataset |
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| A combined segregation and linkage analysis of insulin-dependent diabetes mellitus |
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| HLA haplotype sharing and proband genotype in IDDM |
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| Regional assignments of three polymorphic DNA segments on human chromosome 15 |
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