Newton Ennis Morton population geneticist
Morton, Newton E. 1929-...
Morton, Newton E.
Morton, Newton E. (Newton Ennis), 1929-
Morton, Newton E., 1929-2018
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Morton, Newton E. (Newton Ennis), 1929-2018
VIAF ID: 108616086 (Personal)
Permalink: http://viaf.org/viaf/108616086
Preferred Forms
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100 1 _ ‡a Morton, Newton E
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100 1 _ ‡a Morton, Newton E. (sparse)
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100 1 _
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Morton, Newton E.
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100 1 _ ‡a Morton, Newton E.
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100 1 _ ‡a Morton, Newton E. ‡d (1929- ).
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100 1 _
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Morton, Newton E.
‡d
1929-
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100 1 _
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Morton, Newton E.
‡d
1929-...
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100 1 0
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Morton, Newton E.
‡q
(Newton Ennis),
‡d
1929-
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100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-
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100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-
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100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-2018
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100 1 _
‡a
Morton, Newton E.,
‡d
1929-2018
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100 0 _
‡a
Newton Ennis Morton
‡c
population geneticist
4xx's: Alternate Name Forms (12)
Works
| Title | Sources |
|---|---|
| Computer applications in genetics / ed. by Newton E. Morton. - Honolulu, 1969. |
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| Genetic factors in "schizophrenia." |
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| Genetics of interracial crosses in Hawaii |
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| Major loci for lipoprotein concentrations |
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| The marker (X) syndrome: a cytogenetic and genetic analysis. |
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| Meta-analysis and retrospective collaboration: two methods to map oligogenes for atopy and asthma |
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| Methods in genetic epidemiology |
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| A metric map of humans: 23,500 loci in 850 bands |
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| Multiplex families with two or more probands |
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| Neural tube malformations: complex segregation analysis and calculation of recurrence risks |
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| No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers |
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| Oculoauriculovertebral anomaly: segregation analysis |
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| The optimal measure of allelic association |
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| Origin of human trisomics and polyploids |
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| Origin of sex chromosome aneuploidy. |
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| Parameters of the human genome |
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| Path analysis of family resemblance in the presence of gene-environment interaction |
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| Path analysis under generalized assortative mating. I. Theory |
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| Pharmacokinetic model driven infusion of propofol in children |
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| Phenodeviants and Genetic Homeostasis |
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| Physical mapping by multiple pairwise analysis. |
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| Pingelap and Mokil Atolls: migration |
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| Population genetics and disease control |
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| Population structure of the ABO blood groups in Switzerland |
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| Positional cloning by linkage disequilibrium |
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| Probabilités et hérédité |
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| Problems and methods in the genetics of primitive groups |
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| Proceedings of a conference |
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| Properties of linkage disequilibrium (LD) maps |
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| Quantitative hemagglutination in the ABO system |
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| Racial admixture in north-eastern Brazil |
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| Radiation hybrid mapping |
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| Recollections of James Neel |
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| Recurrence risks in complex inheritance with special regard to pyloric stenosis |
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| Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH region |
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| Relation between homozygous viability and average dominance in Drosophila melanogaster |
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| Reproductive and menstrual history of females with fragile X expansions |
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| Residual family resemblance for PTC taste sensitivity. |
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| Resolution of cultural and biological inheritance by path analysis: Corrigenda and reply to Goldberger letter |
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| Resolution of linkage for irregular phenotype systems |
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| Response to Carothers' letter |
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| A retrospective collaboration on chromosome 5 by the International Consortium on Asthma Genetics |
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| Revisiting Race in a Genomic Age. |
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| The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission |
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| Segregation analysis of balanced pericentric inversions in pedigree data |
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| Segregation analysis of complex phenotypes: an application to schizophrenia and auditory P300 latency. |
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| Segregation analysis of peripheral neurofibromatosis (NF1) |
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| Segregation and linkage analyses of 72 leprosy pedigrees |
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| A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency |
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| Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women |
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| Sex effect on intelligence and mental retardation. |
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| Significance levels in complex inheritance |
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| Significance of maximal lods. |
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| Sinking pre-beta lipoprotein and coronary heart disease in Japanese-American men in Hawaii |
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| Skewness in commingled distributions |
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| A Source book for linkage in man |
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| The Src family tyrosine kinase Fyn regulates natural killer T cell development |
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| Standard maps of chromosome 10. |
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| Studies on locus content mapping |
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| Suggestive evidence for genetic linkage between IgE phenotypes and chromosome 14q markers. |
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| Surveillance of Down's syndrome as a paradigm of population monitoring. |
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| Tables for Testing Significance in a 2 × 2 Contingency Table |
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| Tests of order in multipoint linkage. |
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| Theoretical aspects of population genetics. |
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| Topology of kinship in Micronesia |
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| Toward positional cloning with SNPs |
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| Transition matrices with mutation |
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| Transmission probabilities are not correctly implemented in the computer program POINTER |
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| Trials of structural exploratory data analysis |
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| Trials of the beta model for complex inheritance |
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| Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction |
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| A twin study of intelligence in Russia |
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| The use of map functions in multipoint mapping. |
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| Variability of human linkage data |
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