Someone  please help with each question, they are all about the same pedigree. The first question the option is (DOMINANT OR RECESSIVE) The bottom part of the second image the cut off part asks: "For the next question, give the probability as a fraction that is simplified to the lowest value. Type  your fraction in #/# format without spaces. For example, one-half should be typed as 1/2. Failure to follow these instructions will result in your answer being marked as incorrect.  Suppose that III-4 and III-5 were to have a child. What is the probability that

Make sure to show if it is big (Y) or little (y) Big (S) or little (s) it is so hard to understand if you write it in paper. Please, help me

Joseph is heterozygous for the traits F (dominant to f) and B (dominant to b)and his genes are in cis, and these locuses are on the same chromosome and separated by 30 map units. Sara is also heterozygous for these traits but here genes are in trans. Calculate how likely it would be to observe an individual who is homozygous dominant for the genes F and B. Be sure to show your work for full credit.

A family tree of sorts is called a pedigree. The symbols used for a pedigree are: female, unaffected female, affected ☐male, unaffected male, affected I 11 III 1 Pedigree Chart Minor Peta #2 Siblings are placed in hirth order from left to right and are labeled with Arabic numerals. Each generation is labeled with a Roman numeral. Therefore, the male exhibiting the trait in the pedigree below in the bottom, center would be identified as III-4. 1. Which members of the family above are affected by Huntington's Disease? 4. How many girls did II-1 and 11-2 have? 3. How many children did individuals 1-1 and 1-2 have? 2. There are no carriers for Huntington's Disease- you either have it or you don't. With this in mind, is Huntington's disease caused by a dominant or recessive trait? 5. How are individuals III-2 and II-4 related? 8 -Huntington's Disease

I’m having trouble solving this questions about which is best conclusion answer can you please help?

Mendelian Genetics The presence of a dimple on the cheek is governed by a dominant gene. A couple had already 4 children with dimpled cheeks. What would be the probability of having the next child as another dimpled if both parents are heterozygous for this character? Show your solution using Punnett Square

Can you please not type the answer can you write it on a paper