Given is : $X$ is the chromosome with gene for haemophilia and $X$ is the chromosome with normal gene. Which of the following individuals will act as carrier for haemophilia
Given is : $X$ is the chromosome with gene for haemophilia and $X$ is the chromosome with normal gene. Which of the following individuals will act as carrier for haemophilia
- A
$X^hY$
- B
$X Y$
- C
$X^hX^h$
- D
$X^hX$
Similar Questions
Choose correct option.
$(i)$ The heterozygous female transmit the disease to son.
$(ii)$ Change in the shape of the $RBC$ from biconcave disc to elongated sickle like structure.
$(iii)$ Mentally retarded.
$(iv)$ Heamoglobin not formed proper amount in blood.
Choose correct option.
$(i)$ The heterozygous female transmit the disease to son.
$(ii)$ Change in the shape of the $RBC$ from biconcave disc to elongated sickle like structure.
$(iii)$ Mentally retarded.
$(iv)$ Heamoglobin not formed proper amount in blood.
It is said, that the harmful alleles get eliminated from population over a period of time, yet sickle cell anaemia is persisting in human population. Why ?
It is said, that the harmful alleles get eliminated from population over a period of time, yet sickle cell anaemia is persisting in human population. Why ?
A colour blind man marries the daughter of a colour blind person. Then in their progeny
A colour blind man marries the daughter of a colour blind person. Then in their progeny
- [AIPMT 1988]
Symptoms representing a particular disease due to chromosomal abnormalities are referred to
Among symbol $A, B$ and $C, C$ indicates
Among symbol $A, B$ and $C, C$ indicates