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>
False because extrusive rocks have fine-grained texture due to the rapid cooling of magna above the earth surface. On the other hand extrusive rocks have course grained texture due to slow cooling of magna beneath the Earth's surface
