| mendelian inheritance |
The mode of inheritance of nulear genes, in contrast to "non-Mendelian" or "extra-nuclear" inheritance which is controlled by cytoplasmic heredity determinants. [Source: Agricultural Genome Information System, USDA]
출처: www.cs.uu.nl/people/ronnie/local/genome/m.html
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| mendelian disorder |
Inherited disorder due to a defect in a single gene .
출처: www.bwhct.nhs.uk/clinicalgenetics/glossary.htm
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| mendelian d. |
a genetic disease, showing a mendelian pattern of inheritance, and caused by a single mutation in the structure of DNA, which causes a single basic defect that has some pathological consequence or consequences. Called also monogenic or single-gene d. See also inborn error of metabolism, under error.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| mendelian i. |
see Mendel's laws, under law.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| mendelian l.’s |
Mendel's l's.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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