I believe the correct answer is acid rain.
Pretty sure its secondary waves
The correct answer is: The synaptonemal complex.
Non-sister chromatids are chromatids from two homologous chromosomes. In prophase I of meiosis two homologous chromosomes pair and this pairing is called synapsis. This allows possible crossing over to occur. Two non-sister chromatids are connected in synapsis by a protein-RNA complex called the synaptonemal complex.
Crossing-over or the physical exchange of chromosome parts might occur and bring to genetic recombination. The sites of crossing-over between nonsister chromatids and are called chiasmata.
Answer:
You just gotta light up light up sketchers
Explanation:
Answer: The correct answer to the question is option C
BECAUSE YOU HAVE HAD ONE CHILD WITH TAY-SACHS,YOU MUST EACH CARRY THE ALLELE.ANY CHILD YOU HAVE HAS A 25% CHANCE OF HAVING THE DISEASE.
Explanation: Tay- Sachs is a rare disorder that is inherited,it is characterised by a progressive destruction of the nerves of the brain and spinal cord.its onset is from around 6months of life to around 4-5years of age when the child affected eventually dies.
A Child that have Tay-Sachs experiences problem with coordination,muscle contraction, must stiffness and weakness.there is also difficulty is speaking, swallowing, wasting(uncontrolled weightloss), hearing loss,seizure, and vision loss.
Since the parents of the child in the question claims they don't have Tay- Sachs and no one in the family has it but they came down with a child having Tay-Sachs and one of the major factors to Tay-Sachs as stated above is heredity,the main point to counsel the couples on is that because they have had one child with Tay-Sachs,they most each carry the allele which is obviously recessive so any child they had have has 25% chance of having the disease.
