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  • ventricular septal defect
    ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
  • visual defect
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  • visual field defect
    ½Ã¾ß°á¼Õ
  • window defect
    â¹®ºñħ, â¹®Çü±¤
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  • sensory defect
    °¨°¢°á¼Õ
  • separation defect
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  • septal defect
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  • septation defect
    »çÀ̸·Çü¼º°áÇÔ
  • skull bone defect
    ¸Ó¸®»À°á¼Õ, µÎ°³°ñ°á¼Õ
  • synthesis defect
    ÇÕ¼º°áÇÔ
  • ventricular septal defect
    ½É½Ç»çÀ̸·°á¼Õ, ½É½ÇÁ߰ݰá¼Õ
  • visual defect
    ½Ã°¢°á¼Õ
  • visual field defect
    ½Ã¾ß°á¼Õ
  • wedge shape defect
    ½û±â°á¼Õ
  • window defect
    â¹®ºñħ, â¹®Çü±¤
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  • genetic mucopolysaccharidosis
    À¯Àü¼º ¹«ÄÚ´Ù´çüÁõ.
  • genetic mutation
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  • genetic mutations
    À¯Àü¼º º¯ÀÌ(¡­Ü¨ì¶)
  • genetic prognosis
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  • genetic psychology
    ¹ß»ý½É¸®ÇÐ(Û¡ßæãýìµùÊ).
  • genetic reactivation
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  • genetic reassortment
    À¯ÀüÀÚÀçÆí¼º, À¯ÀüÀÚÀçÁýÇÕ
  • genetic recombination
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  • genetic recombination
    À¯ÀüÀû ÀçÁ¶ÇÕ(¡­î¢ðÚùê).
  • genetic recombination
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  • genetic recombination
    À¯ÀüÀÚÀçÁ¶ÇÕ
  • genetic recombination
    À¯ÀüÀÚ ÀçÁ¶ÇÕ(¡­î¢ðÚùê).
  • genetic regulation
    À¯ÀüÀû Á¶Àý.
  • genetic regulation
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  • genetic resistance
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  • genetic marker
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  • genetic marker
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  • genetic marker
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    À¯ÀüÀû ÀçÁ¶ÇÕ(¡­î¢ðÚùê).
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MTT malignant teratoma, trophoblastic; maximal treadmill test; meal tolerance test; mean transit time; m...
NPT neoprecipitin test; nocturnal penile tumescence; normal pressure and temperature; sodium phosphate t...
PTT partial thromboplastin time; particle transport time; posterior tibial tendon (transfer); prothrombi...
ROT real oxygen transport; remedial occupational therapy; right occipito-transverse [fetal position]
SHTTP secure hypertext transport protocol
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ETS electron transport system
TR transport rate
CancerWEB ¿µ¿µ ÀÇÇлçÀü À¯»ç °Ë»ö °á°ú : 15 ÆäÀÌÁö: 7
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)
genetic disequilibrium A state in the genetic composition of a population which under selection may be expected to change toward an equilibrium or absorbing state.
(05 Mar 2000)
genetic distance <molecular biology> A way of measuring the amount of evolutionary divergence in two separated populations of a species by counting the number of allelic substitutions per locus that have cropped up in each population.
(09 Oct 1997)
genetic diversity <genetics> A property of a community of organisms of a certain species, in which members of the community have variations in their chromosomes due to a large number of slightly dissimilar ancestors, this property makes the community in general more resistant to diseases or to changing ecological conditions.
(09 Oct 1997)
genetic dominance Denoting a pattern of inheritance of an autosomal mendelian trait due to a gene that always manifests itself phenotypically; generally, the phenotype in the homozygote is more severe than in the heterozygote, but details depend on what criterion of phenotyping is used.
Dominance of traits, an expression of the apparent physiologic relationship existing between two or more genes that may occupy the same chromosomal locus (alleles). at a specific locus there are three possible combinations of two allelic genes, A and a: two homozygous (AA and aa) and one heterozygous (Aa). If a heterozygous individual presents only the hereditary characteristic determined by gene A, but not a, A is said to be dominant and a recessive; in this case, AA and Aa, although genotypically distinct, should be phenotypically indistinguishable. If AA, Aa, and aa are distinguishable, each from the others, A and a are codominant.
(05 Mar 2000)
genetic drift <genetics> The random change of the occurance of a particular gene in a population, genetic drift is thought to be one cause of speciation when a group oforganisms is separated from its parent population.
(09 Oct 1997)
genetic engineering <molecular biology, technique> General term covering the use of various experimental techniques to produce molecules of DNA containing new genes or novel combinations of genes, usually for insertion into a host cell for cloning.
(07 May 1998)
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