law of independent assortment

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Words related to law of independent assortment

each member of a pair of homologous chromosomes separates independently of the members of other pairs so the results are random

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References in periodicals archive ?
To knowledge, no approach has been found in literature that provides a quick prediction of genotypic and phenotypic outcome of a particular cross for Mendelian inheritance without the need to draw genotype symbols from both parents through Punnett squares or alternative forked-line method.
Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.
Mendelian inheritance, linkage and genotypic disequilibrium in microsatellite loci isolated from Hymenaea courbaril (Leguminosae).
The two lines C1 and C2 fitted 3:1 Mendelian inheritance, but line C3 did not.
38] OMIM, "Online Mendelian Inheritance in Man," http://www .
2] Nonstandard abbreviations: TLC, thin-layer chromatography; OMIM, Online Mendelian Inheritance in Man.
Electronic Database Information: Online Mendelian Inheritance in Man (OMIM) [http://www.
Chi-square tests were performed for all AFLP amplicons using Mendelian inheritance ratios of 3:1, 1:1 or 1:3.
com)-- In 2005, Susan Lolle and colleagues from Purdue University published a paper in Nature, concluding that Arabidopsis thaliana plants do not obey the laws of Mendelian inheritance (the idea that all genes are inherited from their parents).
Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders, ed 12.
The 2013 release of the Medical Subject Headings (MeSH) includes improvements in a variety of areas including new ingredient identifiers from the FDA, a redesign of the Carboxylic Acids tree structure and new terms from the disease portion of the Online Mendelian Inheritance in Man (OMIM).
The table of contents consists of a chart of information on mode of inheritance, the Mendelian Inheritance in Man number, the locus, the mutated gene, and the affected protein.
The Online Mendelian Inheritance of Man (OMIM), which is well-known data base for genetic diseases and syndromes, also, lists them by different names.
However, much of the emphasis in this regard tends to be directed toward Mendelian inheritance patterns, which are characteristic of genes found on chromosomes within the cell nucleus.