| ERT | esophageal radionuclide transit; estrogen replacement therapy; examination room terminal; external r... |
|---|---|
| ICT | icteric, icterus; indirect Coombs test; inflammation of connective tissue; insulin coma therapy; int... |
| OT | objective test; oblique talus; occlusion time; occupational therapist, occupational therapy; ocular ... |
| ARF | acute renal failure; acute respiratory failure; acute rheumatic fever; Addiction Research Foundation... |
| DAPRU | Drug Abuse Prevention Resource Unit |
acute angle
| genetic information | The heritable biological information coded in the nucleotide sequences of DNA or RNA (certain viruses), such as in the chromosomes or in plasmids. (09 Oct 1997) |
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| genetic isolate | To separate from other persons, materials or objects. (18 Nov 1997) |
| genetic lethal | A disorder that prevents effective reproduction by those affected; e.g., Klinefelter syndrome. (05 Mar 2000) |
| genetic linkage | <genetics> The term refers to the fact that certain genes tend to be inherited together, because they are on the same chromosome. Thus parental combinations of characters are found more frequently in offspring than nonparental. Linkage is measured by the percentage recombination between loci, unlinked genes showing 50% recombination. See: linkage equilibrium, linkage disequilibrium. (18 Nov 1997) |
| genetic load | <genetics> In general terms the decrease in fitness of a population (as a result of selection acting on phenotypes) due to deleterious mutations in the population gene pool. More specifically, the average number of recessive lethal mutations, in the heterozygous state, estimated to be present in the genome of an individual in a population. (18 Nov 1997) |
| genetic locus | <genetics> The position of a gene in a linkage map or on a chromosome. (18 Nov 1997) |
| genetic map | <genetics> A map of the relative positions of genetic loci on a chromosome, determined onthe basis of how often the loci are inherited together. Distance ismeasured in centimorgans (cM). (09 Oct 1997) |
| genetic mapping | Determination of the relative positions of genes on a DNA molecule (chromosome or plasmid) and of the distance, in linkage units or physical units, between them. (14 Nov 1997) |
| genetic marker | A gene which has an easily identifiable phenotype so that one can tell apart cells or individuals which have the gene and those which do not have it. Such a gene can also be used as a probe to mark cell nuclei or chromosomes so that they can easily be isolated or identified from other nuclei or chromosomes later. (09 Oct 1997) |
| genetic markers | A phenotypically recognizable genetic trait which can be used to identify a genetic locus, a linkage group, or a recombination event. (12 Dec 1998) |
| genetic material | A gene, a part of a gene, a group of genes, or fragments of many genes, on a molecule of DNA, a fragment of DNA, a group of DNA molecules, or fragments of many DNA molecules. Could refer to anything from a small fragment of DNA to the entire genome of an organism. (09 Oct 1997) |
| genetic model | A formalised conjecture about the behaviour of a heritable structure in which the component terms are intended to have literal interpretation as standard structures of empirical genetics. (05 Mar 2000) |
| genetic penetrance | The extent to which a genetically determined condition is expressed in an individual. (05 Mar 2000) |
| genetic polymorphism | The occurrence in the same population of multiple discrete alletic states of which at least two have high frequency (conventionally of 1% or more). (05 Mar 2000) |
| genetic psychology | A science dealing with the evolution of behaviour and the relation to each other of the different types of mental activity. (05 Mar 2000) |