Alkaptonuria is an inborn biochemical disorder in which the person excretes:
A.Albumen
B.Homogentisic acid
C.HCI
D.Acetic acid
A.Albumen
B.Homogentisic acid
C.HCI
D.Acetic acid
A.Dominant autosomal
B.Recessive
C.Confined to males
D.None of these
A.A
B.B
C.AB
D.O
A.2;1
B.1.1
C.3;5
D.1;2
A.All of the blood groups
B.Only A and B – group
C.AB and O – group
D.AB only
A.44 + XY
B.2A + XY
C.44 + 1 + 1
D.Both (a) & (b)
A.Phenylalanine oxidase
B.Phenylalanine hydroxylase
C.Phenylalanine phosphorylase
D.Phenylalanine transmutase
A.Hereditory disease
B.Contagious disease
C.Deficiency disease
D.Sex-linked disease
A.A
B.B
C.AB
D.O
A.Aneuploidy
B.Euploidy
C.Polyphridy
D.None of these