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An autosomal trait will occur with equal frequency in both males and females?
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∙ 13y ago
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∙ 13y ago
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Cystic fibrosis autosomal dominant?
hey I'm not positive but I believe that Cystic Fibrosis is autosomal. My reasonning for this is that there seems to be an equal number of females that have cystic fibrosis as there are males. I AM NOT POSITIVE.
Assume that a particular genetic condition in a mammalian species causes an inability to digest starch This disorder occurs with equal frequency in males and females in most cases neither parent is af?
This genetic condition is likely an autosomal recessive trait since it occurs with equal frequency in males and females. If neither parent is affected, it suggests that both parents are carriers of the condition. In order for a child to be affected, they would need to inherit two copies of the recessive allele, one from each carrier parent.
Which is true of autosomal recessive diseases a. The disease can skips generations b. Males and Females have an equal chance of inheriting the mutant allele c. Only Males inherit the?
only A and B
Who can be carrier of autosomal disorder?
females
What is an autosomal dominant disorder?
Chromosomes can be divided into autosomes and sex chromosomes. The sex chromosomes (eg X and Y in humans) carry genes concerned with sex determination. The remaining chromosomes are called autosomes. They carry genes which are the same in males and females. Aberrations are changes or mutations in the chromosomes. So autosomal aberrations are mutations in the non-sex chromosomes.
Cystic fibrosis autosomal dominant?
hey I'm not positive but I believe that Cystic Fibrosis is autosomal. My reasonning for this is that there seems to be an equal number of females that have cystic fibrosis as there are males. I AM NOT POSITIVE.
Assume that a particular genetic condition in a mammalian species causes an inability to digest starch This disorder occurs with equal frequency in males and females in most cases neither parent is af?
This genetic condition is likely an autosomal recessive trait since it occurs with equal frequency in males and females. If neither parent is affected, it suggests that both parents are carriers of the condition. In order for a child to be affected, they would need to inherit two copies of the recessive allele, one from each carrier parent.
Which is true of autosomal recessive diseases a. The disease can skips generations b. Males and Females have an equal chance of inheriting the mutant allele c. Only Males inherit the?
only A and B
Is sickle cell anemia a sexlinked trait?
Nope! The disease is equally in both males and females. This means that it is autosomal.
Is sickle cell anemia a sex link trait?
Nope! The disease is equally in both males and females. This means that it is autosomal.
What are the demographics for Refsum disease?
Refsum disease is an extremely rare disorder that affects males and females with equal frequency. It has been observed in Norwegian populations as well as others.
What type of hereditary condition is Paramyotonia congenita?
Paramyotonia congenita is passed on in families as an autosomal dominant trait. This means that males and females are affected equally
Who can be carrier of autosomal disorder?
females
What is the role of heredity in myotonic dystrophy?
DM is inherited through autosomal dominant inheritance. This means that equal numbers of males and females are affected. It also means that only one gene in the pair needs to have the mutation in order for a person to be affected.
How many homologous chromosomes do males have?
Males have 44 homologous chromosomes, or 22 pairs. Females are 46 and 23 respectively since they have homologous sex chromosomes.
Why did women suffrage occur?
So that females and males would be equal.
Where does Gaucher disease occur most often?
Gaucher disease is found in populations all over the world (20,00 to 40,000 people have a type of the disease), and it occurs with equal frequency in males and females.
