Polygenic inheritance result in a continuum of phenotypes because the genes that are involved can be considered to be co-dominant traits that fall into discrete categories are called continuous traits false.
<h3>What is Polygenic Inheritance?</h3>
A single inherited phenotypic trait that is governed by two or more separate genes is referred to as polygenic inheritance, often referred to as quantitative inheritance.
In a system that is distinct from Mendelian Genetics, wherein monogenic features are determined by the various alleles of a single gene, polygenetic traits may exhibit a variety of potential phenotypes, determined by a number of different genes and the interactions between them.
In contrast to Mendelian genetics, when one allele completely dominates or hides another, features generated by polygenic inheritance are not only the result of dominance and recessively. Instead, polygenic features show incomplete dominance, resulting in a combination of the phenotypes seen in the parents in the offspring.
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<span>The greatest incidence of osteoporosis will be found in the menopausal women.</span>
<span>Osteoporosis
can occur in both men and women and at any age, but it is most common in older
women. Osteoporosis cane defined as a disease with increased bone weakness. It
is the most common cause of a broken bone among the elderly and it is followed
by chronic pain and a decreased ability to carry out normal activities.</span>
Answer:
Explanation:
A cell with two pairs of each set of chromosomes is called a [ diploid / haploid ] cell.
Answer:
Option A, They have enzymatic properties that can covalently modify DNA.
Explanation:
Histones have very basic nature and possess no enzymatic properties. However, any modification of DNA is carried out after the end of translation process with the help of enzymes on the N –terminal tails through processes such methylation, acetylation, citrullination, phosphorylation.
There are several Histone-modifying enzymes in the human genome that interact with the non-histone proteins to form functional complexes
Hence, option A is correct
In anaphase I, homologouspairs are separated but sister chromatids stay joined together. <span>The "I" in anaphase I refers to the first round of cell division, which resembles ordinary mitosis. So in anaphase I, the homologous pairs separate but the sister chromatids stay together. Then the cell goes directly into a second round of cell division - in anaphase II, the sister chromatids are separated into four (now haploid) cells.</span>
