CBSE
A normal woman is married with a man having hypertrichosis condition. They got one daughter and one son. What is the possibility of this daughter to have hypertrichosis condition?
0%
25%
50%
100%
A colourblind mother and normal father would have
colourblind sons and normal/carrier daughters
colourblind sons and daughters
all colourblind
all normal
Mirabilis jalapa shows
codominance
incomplete dominance
dominance
complementary genes
Which of the following is a test cross ?
Tt x tt
TT x tt
Tt x Tt
tt x tt
A woman has a haemophilic son and three normal children. Her genotype and that of her husband with respect to this gene would be
XX and XhY
XhXh and XhY
XhXh and XY
XhX and XY
Autosomes in humans are
11 pairs
22 pairs
23 pairs
43 pairs
The trisomy for 21st chromosome is called
Down's syndrome
Turner's syndrome
Sickle cell anaemia
Klinefelter's syndrome
Tay Sach's disease is due to
sex linked recessive gene
sex linked dominant gene
autosomal dominant gene
autosomal recessive gene
Which of the following is not related to sex chromosome X or Y?
Turner's syndrome
Klinefelter's syndrome
Down's syndrome
Haemophilia and colour bindness
1 : 2 : 1 phenotypic and genotypic ratio is found in
complementary genes
blending inheritance
multiple alleles
pseudo alleles