| genomic imprint |
The inactivation of a gene by its allele.
Ãâó:
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|---|---|
| genomic i. |
differential expression of a gene or genes as a function of whether they were inherited from the male or the female parent, e.g., a deletion on chromosome 15 that causes Prader-Willi syndrome if inherited from the father causes instead Angelman's syndrome if inherited from the mother.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| genomic m. |
a mutation affecting the number of chromosomes present, e.g., aneuploidy, in which the genome gains or loses one or more chromosomes, and polyploidy, in which the overall chromosome number is doubled or tripled. See also chromosomal m. and point m.
Ãâó: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| genomics |
The analysis of the entire genome of a chosen organism.
Ãâó: www.syrrx.com/technology/glossary.htm
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| genome |
The complete genetic content of an organism.
Ãâó: www.syrrx.com/technology/glossary.htm
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