| EIM | excitability-inducing material |
|---|---|
| GIM | general internal medicine; gonadotropin-inhibiting material |
| HAZ | MAT hazardous material |
| ILM | insulin-like material; internal limiting membrane |
| MSD | material safety data; mean square deviation; mild sickle cell disease; most significant digit; multi... |
| 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 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) |
| genetic recombination | <molecular biology> Formation of new combinations of alleles in offspring (viruses, cells or organisms) as a result of exchange of DNA sequences between molecules. It occurs naturally, as in crossing over between homologous chromosomes in meiosis or experimentally, as a result of genetic engineering techniques. (18 Nov 1997) |
| genetic screening | The process of testing individuals to find out if they carry genes for certain known genetic diseases, such as sickle cell anaemia. (09 Oct 1997) |
| genetic techniques | Chromosomal, biochemical, intracellular, and other methods used in the study of genetics. (12 Dec 1998) |
| genetic testing | Identifying foetuses or infants afflicted with hereditary diseases or conditions, and carriers of recessive disorders by means of DNA analysis. See: DNA markers, familial screening, prenatal screening. Synonym: genetic testing. (05 Mar 2000) |