Achondroplasia is a common form of dwarfism caused by an autosomal dominant mutation in the fibroblast growth factor receptor 3
(FGFR3) gene. Two copies of the mutant gene are invariably fatal before or shortly after birth. If a person with achondroplasia marries a person of normal height, what is the probability that they will have a child with achondroplasia?
Achondroplasia is caused about by a quality change (transformation) in the <em>FGFR3 gene</em>
The <em>FGFR3 quality</em> makes a protein called fibroblast development factor <em>receptor 3 </em>that is engaged with changing over ligament to bone
<em>FGFR3</em> is the main quality known to be related with <em>achondroplasia Achondroplasia</em> is acquired in an autosomal predominant example, which implies one duplicate of the adjusted quality in every cell is adequate to<em> cause the confusion</em>
In the rest of the cases, individuals with <em>achondroplasia </em>have acquired an adjusted <em>FGFR3 quality</em> from a couple of <em>affected parents</em>
D. Division of body cells results in a greater variety of traits
Explanation:
Since sexual reproduction occurs between two organisms their traits are combined to form a new individual who has similarities and differences to both parents.
It's a great tree for small properties because you only need one to produce fruit. Pluots are similar fruits. ... The seeds from the cross-pollinated fruit produce a different type of tree that has some characteristics of both trees.
