| 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.
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| mendelian i. |
see Mendel's laws, under law.
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| mendelian l.’s |
Mendel's l's.
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| mendelian r. |
an expression of the occurrence of distinctly contrasted mendelian characters in succeeding generations of hybrid offspring.
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| mendelian t. |
see Mendel's laws, under law.
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