Which one of the following is a genetically transmitted character
- AColour blindness
- BHydrocephalus
- CHemophilia
- DAll of these.
Similar Questions
If mother is a carrier for colour blindness and father is normal, then in the offsprings this disease may be seen in
If mother is a carrier for colour blindness and father is normal, then in the offsprings this disease may be seen in
- [AIPMT 1999]
If a haemophilic man marries a woman carrier (heterozygous) for haemophilia, what would be the possibility that their daughter would be haemophilic
If a haemophilic man marries a woman carrier (heterozygous) for haemophilia, what would be the possibility that their daughter would be haemophilic
:Match the columns :
Column $I$
Column $II$
$(a)$
Sickle cell anaemia
$(p)$
Homogentisic acid
$(b)$
Alkaptonuria
$(q)$
Lack of Melanin
$(c)$
Albinism
$(r)$
Accumulation of Amino acid
$d)$
Phenyl Ketonuria
$(s)$
Defective haemoglobin
:Match the columns :
| Column $I$ |
Column $II$ |
||
| $(a)$ | Sickle cell anaemia | $(p)$ | Homogentisic acid |
| $(b)$ | Alkaptonuria | $(q)$ | Lack of Melanin |
| $(c)$ | Albinism | $(r)$ | Accumulation of Amino acid |
| $d)$ | Phenyl Ketonuria | $(s)$ | Defective haemoglobin |
Which of the following abnormalities is due to autosomal dominant mutation?
Which of the following abnormalities is due to autosomal dominant mutation?
Which of the following is not correct option for Phenylketonuria ?
Which of the following is not correct option for Phenylketonuria ?