Answer:
PpDD and PpDd
Explanation:
Pigmented eyes (P) are dominant to non-pigmented (p), and dimpled chins (D) are dominant to Non-dimpled chins (d).
The <u>possible genotypes of a pigment-eyed, dimple-chinned person</u> would be PPDD, PpDd, PPDd, PpDD while a blue-eyed person without a dimpled chin would have the genotype ppdd.
The genotype of a blue-eyed, dimpled chin child would be either of ppDd or ppDD, but in this case, the mother is ppdd and as such, the child cannot have two copies of D allele. Hence, the genotype of the child can only be ppDd.
In order for the child to have blue eyes (pp), it means that the father has to have the non-pigmented allele (p). This also means that the father is heterozygous for eye pigmentation (Pp).
<em>Hence, the genotype of the father is now limited to </em><em>PpDD</em> <em>and </em><em>PpDd</em>.
Vast away of industries, like the other person said they said more
Answer: In Stage 4 of the Demographic Transition Model birth rates and death rates are both low, stabilizing total population growth. The decline in both birth and death rates of most Stage 4 countries have been attributed to strong economies, highly educated citizens, ample healthcare systems, the migration of people from rural communities to cities (Bulgaria)
Explanation: i dont know if it's correct to them
our thyroid glands plays a main role in a human body. It secretes thyroxine and calcitonin. In which thyroxine help in growth and cellular metabolism and calcitonin helps to regulates calcium concentration in blood . If thyroid gland stops working then there is low level of calcium in our blood, which leads to mental and hormonal disorder. In this way a person's blood calcium level would be affected if his/her thyroid gland stops working.
I) Locus- the chromosomal site where a specific gene is located. A locus is a fixed position on a chromosome, like the position of a gene or a marker. Each chromosome carries ,many genes; human's estimated haploid (n) protein coding genes are about 20,000, on the 23 different chromosomes.
ii) Interference; the observed double crossover frequency differs from the expected double crossover frequency. Cross over interference is used to refer to the non-random placement of crossovers with respect to each other during meiosis. It results in widely spaced crossovers along chromosomes. Interference may exert its effect across whole chromosomes. As chromosomes in many eukaryotes are large, interference must be able to act over megabase lengths of DNA.
iii) Linkage- the tendency for genes located in close proximity on the same chromosome to be inherited together. Normally when two genes are close together on the same chromosome, they do not assort independently and are said to be linked. Whereas genes located on different chromosomes assort independently and have a recombination frequency of 50%, linked genes have a recombination frequency that is less than 50%.
iv) Recombination- the process by which a new pattern of alleles on a chromosome is generated. Genetic recombination is the production of offspring with combinations f traits that differ from those found in either parent. During meiosis in eukaryotes, genetic recombination involves the pairing of homologous chromosomes. This may be followed by information transfer between the chromosomes.
