MCQ Book Questions

Q52040. All the following statements about restriction fragment length polymor- phism are true except

Q52041. Inborn errors of urea cycle can cause all the following except

Q52042. Hyperammonaemia type I results from congenital absence of

Q52043. Congenital deficiency of ornithine transcarbamoylase causes

Q52044. A ketogenic amino acid among the fol- lowing is

Q52045. Carbon skeleton of the following amino acid can serve as a substance for gluconeogenesis

Q52046. N-Formiminoglutamate is a metabolite of

Q52047. Methylmalonyl CoA is a metabolite of

Q52048. Homogentisic acid is formed from

Q52049. Maple syrup urine disease results from absence or serve deficiency of

Q52050. Which of the following is present as a marker in lysosomal enzymes to direct them to their destination?

Q52051. Marfan’s syndrome results from a mutation in the gene coding:

Q52052. All the following statements about fibronectin are true except

Q52053. Fibronectin has binding sites for all of the following except

Q52054. Fibronectin is involved in

Q52055. Glycoproteins are marked for destruction by removal of their

Q52056. Glycophorin is present in cell membranes of

Q52057. Selectins are proteins that can recognise specific

Q52058. Hunter’s syndrome results from absence of

Q52059. A cancer cell is characterized by