Answer:
<em>fragile X syndrome </em>
Explanation:
<em>FMR1 gene mutations</em><em> trigger fragile X syndrome.</em>The gene FMR1 offers instructions on how to make a protein called FMRP.
This gene helps to control the output of other proteins and plays a part in the growth of synapses that are specific nerve cell connections.
It creates a <em>variety of developmental issues including intellectual disabilities and cognitive impairment.</em> This disease usually affects males more significantly than women.
When a cell undergoing cellular division identifies that a chromosome misalignment had taken place the cell cycle stops until the error it's corrected.
Option two of the question states that the cell cycle will <u>proceed uncontrollably, this is not the case for the error at hand</u>. Although this can be a problem for cells and leads to the appearance of cancer, it is not caused by chromosome misalignment. As is the case with options 3 and 4.
The stop or delay in the <u>cell cycle is what normally takes place in these situations.</u> This stoppage is done by the <em><u>spindle checkpoint</u></em>, which prevents <u>duplicate chromosomes from separating.</u>
During this time, the error it's corrected. If a cell is not able to correct the error at this time, many situations can follow. <u>However, the most likely is that the cell will undergo a <em>programmed cellular death.</em> </u>
To learn more visit:
brainly.com/question/6856672?referrer=searchResults
A chemical sedimentary rock?
Answer:
I think this should be the chart you were interested in...
Explanation:
Individual Shape in shaded
phenotype pedigrees
Male with gen. TT PTC taster square No
Male with gen. Tt PTC taster square No
Male with gen. tt Non-taster square Yes
Female with gen. TT PTC taster Circle No
Female with gen. Tt PTC taster Circle No
Female with gen. tt Non-taster Circle Yes
*gen- genotype