11 found
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  1.  43
    Insensitivity of the analysis of variance to heredity-environment interaction.Douglas Wahlsten - 1990 - Behavioral and Brain Sciences 13 (1):109-120.
  2.  11
    Some logical fallacies in the classical ethological point of view.Douglas Wahlsten - 1979 - Behavioral and Brain Sciences 2 (1):48-49.
  3.  27
    Race, the heritability of IQ, and the intellectual scale of nature.Douglas Wahlsten - 1980 - Behavioral and Brain Sciences 3 (3):358-359.
  4.  21
    Bias and sampling error in sex difference research.Douglas Wahlsten - 1988 - Behavioral and Brain Sciences 11 (2):214-214.
  5.  14
    Each behavior is a product of heredity and experience.Douglas Wahlsten - 1984 - Behavioral and Brain Sciences 7 (4):699-700.
  6.  20
    Effect sizes and meta-analysis indicate no sex dimorphism in the human or rodent corpus callosum.Douglas Wahlsten & Katherine M. Bishop - 1998 - Behavioral and Brain Sciences 21 (3):338-339.
    Sex dimorphism occurs when group means differ by four or more standard deviations. However, the average size of the corpus callosum is greater in males by about one standard deviation in rats, 0.2 standard deviation in humans, and virtually zero in mice. Furthermore, variations in corpus callosum size are related to brain size and are not sex specific.
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  7.  9
    Goals and methods: The study of development versus partitioning of variance.Douglas Wahlsten - 1990 - Behavioral and Brain Sciences 13 (1):146-161.
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  8.  14
    Indeterminacy is inherent in an inadequate model of evolution, not in nature.Douglas Wahlsten - 1981 - Behavioral and Brain Sciences 4 (2):255-257.
  9.  24
    Sociobiology flops again.Douglas Wahlsten - 1993 - Behavioral and Brain Sciences 16 (2):310-311.
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  10.  1
    Science or prejudice?Douglas Wahlsten - 1989 - Behavioral and Brain Sciences 12 (3):546-547.
  11.  33
    The genetic kaleidoscope of vision.Douglas Wahlsten - 1995 - Behavioral and Brain Sciences 18 (3):490-492.
    Site-specific phenotypic effects of the 73 known alleles in the rhodopsin gene that cause retinal degeneration are difficult to interpret because most alleles are documented in only one case or one family, which means variation in effects could actually arise from interactions with other loci. However, sample sizes necessary to detect epistatic interaction may place an answer to this question beyond our grasp.
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