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  • genetic
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  • genetic
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  • genetic block
    À¯ÀüÀû Â÷´Ü(ë¶îîîÜó´Ó¨).
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  • genetic cause
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  • genetic code
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    À¯Àü»ó´ã(¡­ßÓÓÈ).
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  • genetic defect
    À¯ÀüÀû °áÇÔ(¡­ÌÀùè).
  • genetic defect
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  • genetic defect
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GM gastric mucosa; Geiger-Muller [counter]; general medicine; genetic manipulation; geometric mean; gia...
GP gangliocytic paraganglioma; gastroplasty; general paralysis, general paresis; general practice, gene...
GT gait training; galactosyl transferase; gastrostomy; generation time; genetic therapy; gingiva treatm...
HGMCR human genetic mutant cell repository
IGA infantile genetic agranulocytosis
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MGE mobile genetic element
ASTM American Society for Testing and Materials
ET Exercise Testing
EST Exercise stress testing
ETT Exercise treadmill testing
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genetic assimilation <genetics> A situation in which a characteristic that is normally expressed only in certain environmental situations becomes fixed in a population so that it no longer requires environmental factors to be expressed.
(07 May 1998)
genetic association The occurrence together in a population, more often than can be readily explained by chance, of two or more traits of which at least one is known to be genetic.
(05 Mar 2000)
genetic block <biochemistry, molecular biology> An obstruction in a biochemical pathway caused by a mutation that has crippled production of an enzyme critical to the pathway.
(07 May 1998)
genetic burden The genetic debt due to harmful mutation but as yet undischarged. (In a large population of fixed size every mutation with diminished genetic fitness will eventually become extinct and depending on the details of inheritance and phenotype must be paid for by a fixed number of genetic deaths per mutation, the genetic debt.)
(05 Mar 2000)
genetic carrier An unaffected heterozygote bearing a usually harmful recessive gene, a cancer that bears a dominant but latent age-dependent trait to have offspring with unbalanced karyotypes.
(05 Mar 2000)
genetic code <molecular biology> Relationship between the sequence of bases in nucleic acid and the order of amino acids in the polypeptide synthesised from it. A sequence of three nucleic acid bases (a triplet) acts as a codeword (codon) for one amino acid.
(18 Nov 1997)
genetic colonisation <molecular biology> The process of a parasite (such as a virus) inserting genes into a host's genome which cause the host cell to synthesise products that are only useful to the parasite.
(07 May 1998)
genetic complement <biology, genetics> The set of chromosomes contained within any one particular cell.
(07 May 1998)
genetic complementation <genetics> The reappearance of wild-type characteristics in a cell or organism that has had two distinct mutations on the same chromosome.
Two normal versions of two different mutant genes on different chromosomes affecting the same phenotype which, when inherited together, results in the wild-type phenotype despite the presence of mutant copies of the genes.
(09 Oct 1997)
genetic complementation test A test used to determine whether or not complementation (compensation in the form of dominance) will occur in a cell with a given mutant phenotype when another mutant genome, encoding the same mutant phenotype, is introduced into that cell.
(12 Dec 1998)
genetic compound In medical genetics, the presence of two different mutant alleles at the same loci.
Synonym: genetic compound.
(05 Mar 2000)
genetic counseling <genetics> The genetic testing of couples who are planning to be parents in which their genomes are evaluated and they are given advice or information from a specialist regarding the likelihood of them having children with genetic diseases or defects.
(07 May 1998)
genetic death Death of the bearer of a gene at any age before generating living offspring. May be compatible with good health and long life.
See: genetic lethal.
(05 Mar 2000)
genetic determinant Any antigenic determinant or identifying characteristic, particularly those of allotypes.
Synonym: genetic marker.
(05 Mar 2000)
genetic disease <biology, genetics> A disease, such as cystic fibrosis, that has its origin in changes to the genetic material, DNA.
Usually refers to diseases that are inherited in a Mendelian fashion, although noninherited forms of cancer also result from DNA mutation.
(07 May 1998)
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genetic testing This type of testing involves the examination of an individual's DNA. Also known as gene testing and DNA testing. Learn more about genetic testing.
Ãâó: www.biobasics.gc.ca/english/View.asp
genetic testing tests performed to see if a person has certain gene changes known to increase cancer risk. Such testing is not recommended for everyone, rather for those with specific types of family history. Genetic counseling should be part of the process as well.
Ãâó: www.cancer.org/docroot/GRY/GRY_0.asp
genetic testing A technique used to determine whether a person (or other organism) has a disease causing allele of a certain gene. Identifies people at risk for a specific genetic disease or at risk for transmitting such a disease to their children.
Ãâó: www.med.nyu.edu/rcr/rcr/glossary.html
genetic testing Tests to determine characteristics of genes done to establish a diagnosis or provide genetic counseling.
Ãâó: www.understandingnf1.org/glossary/
genetic testing A technique used to determine whether a person or organism has a certain gene.
Ãâó: www.exploratorium.edu/genepool/glossary.html
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