The genetic fault that usually causes colour vision deficiency is passed on in what's known as an X-linked inheritance pattern.
This means:
1) it mainly affects boys, but can affect girls in some cases
2) girls are usually carriers of the genetic fault – this means they can pass it on to their children, but do not have a colour vision deficiency themselves
3) it's usually passed on by a mother to her son – the mother will often be unaffected as she'll normally just be a carrier of the genetic fault
4) fathers with a colour vision deficiency will not have children with the problem unless their partner is a carrier of the genetic fault
5) it can often skip a generation – for example, it may affect a grandfather and their grandson
6) girls are only affected if their father has a colour vision deficiency and their mother is a carrier of the genetic fault
Answer:
weak acid
Explanation:
4-6.9 belongs to weak acids
Answer:
Individuals who are heterozygous for co-dominant traits show in their phenotype both traits, without mixing.
Explanation:
Codominance is a type of inheritance that does not follow the rules of Mendelian inheritance, characterized by the absence of recessive traits and two different alleles for a character that behave as dominant.
Heterozygous individuals can be observed in codominance that show two different characteristics in their phenotype, without mixing, such as cattle with spotted skin or two colored flowers.