Newton Ennis Morton population geneticist
Morton, Newton E. 1929-...
Morton, Newton E. (Newton Ennis), 1929-
Morton, Newton E.
Morton, Newton E., 1929-2018
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Morton, Newton E. (Newton Ennis), 1929-2018
VIAF ID: 108616086 ( Personal )
Permalink: http://viaf.org/viaf/108616086
Preferred Forms
-
100 1 _ ‡a Morton, Newton E
-
100 1 _
‡a
Morton, Newton E.
-
100 1 _ ‡a Morton, Newton E.
-
100 1 _ ‡a Morton, Newton E. (sparse)
-
100 1 _ ‡a Morton, Newton E. ‡d (1929- ).
-
100 1 _
‡a
Morton, Newton E.
‡d
1929-
-
100 1 _
‡a
Morton, Newton E.
‡d
1929-...
-
100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-
-
100 1 0
‡a
Morton, Newton E.
‡q
(Newton Ennis),
‡d
1929-
-
100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-
-
100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-
-
100 1 _ ‡a Morton, Newton E. ‡q (Newton Ennis), ‡d 1929-2018
-
100 1 _
‡a
Morton, Newton E.,
‡d
1929-2018
-
100 0 _
‡a
Newton Ennis Morton
‡c
population geneticist
4xx's: Alternate Name Forms (11)
Works
| Title | Sources |
|---|---|
| Computer applications in genetics / ed. by Newton E. Morton. - Honolulu, 1969. |
|
| Genetics of interracial crosses in Hawaii |
|
| LODs past and present. |
|
| Major loci for lipoprotein concentrations |
|
| The marker |
|
| Meta-analysis and retrospective collaboration: two methods to map oligogenes for atopy and asthma |
|
| Methods in genetic epidemiology |
|
| Multipoint mapping and the emperor's clothes. |
|
| Neural tube malformations: complex segregation analysis and calculation of recurrence risks |
|
| No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers. |
|
| Oculoauriculovertebral anomaly: segregation analysis |
|
| The optimal measure of allelic association |
|
| Origin of human trisomics and polyploids. |
|
| Origin of sex chromosome aneuploidy. |
|
| Parameters of the human genome |
|
| Path analysis of family resemblance in the presence of gene-environment interaction |
|
| Path analysis under generalized assortative mating. I. Theory |
|
| Pharmacokinetic model driven infusion of propofol in children |
|
| Phenodeviants and Genetic Homeostasis. |
|
| Physical mapping by multiple pairwise analysis. |
|
| Pingelap and mokil atolls: genealogy |
|
| Population genetics and disease control. |
|
| Population structure of the ABO blood groups in Switzerland |
|
| Positional cloning by linkage disequilibrium. |
|
| Probabilités et hérédité |
|
| Problems and methods in the genetics of primitive groups. |
|
| Proceedings of a conference |
|
| Properties of linkage disequilibrium (LD) maps |
|
| Quantitative hemagglutination in the ABO system |
|
| Racial admixture in north-eastern Brazil. |
|
| Radiation hybrid mapping |
|
| Recollections of James Neel. |
|
| Recurrence risks in complex inheritance with special regard to pyloric stenosis |
|
| Refined association mapping for a quantitative trait: weight in the H19-IGF2-INS-TH region. |
|
| Relation between homozygous viability and average dominance in Drosophila melanogaster |
|
| Reproductive and menstrual history of females with fragile X expansions |
|
| Residual family resemblance for PTC taste sensitivity. |
|
| Resolution of cultural and biological inheritance by path analysis: Corrigenda and reply to Goldberger letter |
|
| Resolution of linkage for irregular phenotype systems. |
|
| Response to Carothers' letter. |
|
| A retrospective collaboration on chromosome 5 by the International Consortium on Asthma Genetics |
|
| Revisiting Race in a Genomic Age. |
|
| The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission. |
|
| Segregation analysis of balanced pericentric inversions in pedigree data |
|
| Segregation analysis of complex phenotypes: an application to schizophrenia and auditory P300 latency. |
|
| Segregation analysis of peripheral neurofibromatosis (NF1) |
|
| Segregation and linkage analysis of 40 multiplex multiple sclerosis families. |
|
| A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency |
|
| Serum concentrations of follicle stimulating hormone may predict premature ovarian failure in FRAXA premutation women |
|
| Sex effect on intelligence and mental retardation. |
|
| Significance levels in complex inheritance. |
|
| Significance of maximal lods. |
|
| Sinking pre-beta lipoprotein and coronary heart disease in Japanese-American men in Hawaii |
|
| Skewness in commingled distributions. |
|
| A Source book for linkage in man |
|
| The Src family tyrosine kinase Fyn regulates natural killer T cell development |
|
| Standard maps of chromosome 10. |
|
| Studies on locus content mapping |
|
| Suggestive evidence for genetic linkage between IgE phenotypes and chromosome 14q markers. |
|
| Surveillance of Down's syndrome as a paradigm of population monitoring. |
|
| Tables for Testing Significance in a 2 × 2 Contingency Table. |
|
| Tests of order in multipoint linkage. |
|
| Theoretical aspects of population genetics. |
|
| Topology of kinship in Micronesia |
|
| Toward positional cloning with SNPs |
|
| Transmission probabilities are not correctly implemented in the computer program POINTER |
|
| Trials of structural exploratory data analysis |
|
| Trials of the beta model for complex inheritance |
|
| A twin study of intelligence in Russia |
|
| The use of map functions in multipoint mapping. |
|
| Variability of human linkage data |
|
