Answer:
the answers is yes
Explanation:
because it changes the genetic code, and genetic code is the genes and they define who you are amd wat u look like
Answer:
B. It allows for genetic variation.
Explanation:
As prophase progresses, homologous chromosomes come to lie side by side and become intertwined rather like a zipper. This process is called synapsis. During synapsis, homologous chromosomes exchange genetic material between one another which allows for genetic variation. This exchange is called crossing over.
Answer:
The girls with polydactyly color-blind and is 1/8, the boys with normal fingers and color vision is 1/8.
Explanation:
X - linked recessive trait may be defined as the trait that are normally passes down from mother to son. Males have high chances since they have only one X chromosme. The female should have both X chromosome affected to express the trait. Autosomal dominant trait express the trait in both the homozygous dominant and heterozygous condition.
The red - green color blinded male with polydactylous is married with female that have normal color vision and normal toes and finger. With the help of pedigree chart and probability,the outcome of their children with specific phenotype can be calculated.
Martha is normal for poldactyly and contains recessive trait for polydactyly. She is a carrier for the color blindness as his father is affected by the disease. Bill is affected by the color blindness and heterozygous for the polydactyly trait. The marriage between marry and bill have the children with 1/8 proportion of the girls can be color bind and shows polydactyly {1/4 ( girls with color blindness) × 1/2 ( the probability of polydactyly}. 1/8 proportion of the boys with normal vision and normal toes and finger {1/4 (boys are normal) × 1/2 ( the probability of normal toes and finger}.
