[["Question: Tay-Sachs disease is caused by deficiency of _________________?\nChoices:\nA. Alpha-L-iduronidase\nB. Glucose-6-phosphatase\nC. Hexosaminidase A\nD. Homogentisic acid oxidase\nAnswer:", " Alpha-L-iduronidase"], ["Question: Tay-Sachs disease is caused by deficiency of _________________?\nChoices:\nA. Alpha-L-iduronidase\nB. Glucose-6-phosphatase\nC. Hexosaminidase A\nD. Homogentisic acid oxidase\nAnswer:", " Glucose-6-phosphatase"], ["Question: Tay-Sachs disease is caused by deficiency of _________________?\nChoices:\nA. Alpha-L-iduronidase\nB. Glucose-6-phosphatase\nC. Hexosaminidase A\nD. Homogentisic acid oxidase\nAnswer:", " Hexosaminidase A"], ["Question: Tay-Sachs disease is caused by deficiency of _________________?\nChoices:\nA. Alpha-L-iduronidase\nB. Glucose-6-phosphatase\nC. Hexosaminidase A\nD. Homogentisic acid oxidase\nAnswer:", " Homogentisic acid oxidase"], ["Question: If an X-linked recessive disorder is in Hardy-Weinberg equilibrium and the incidence in males equals 1 in 100, then the expected incidence of affected homozygous females would be _______.\nChoices:\nA. 1 in 1000\nB. 1 in 4000\nC. 1 in 10 000\nD. 1 in 40 000\nAnswer:", " 1 in 1000"], ["Question: If an X-linked recessive disorder is in Hardy-Weinberg equilibrium and the incidence in males equals 1 in 100, then the expected incidence of affected homozygous females would be _______.\nChoices:\nA. 1 in 1000\nB. 1 in 4000\nC. 1 in 10 000\nD. 1 in 40 000\nAnswer:", " 1 in 4000"], ["Question: If an X-linked recessive disorder is in Hardy-Weinberg equilibrium and the incidence in males equals 1 in 100, then the expected incidence of affected homozygous females would be _______.\nChoices:\nA. 1 in 1000\nB. 1 in 4000\nC. 1 in 10 000\nD. 1 in 40 000\nAnswer:", " 1 in 10 000"], ["Question: If an X-linked recessive disorder is in Hardy-Weinberg equilibrium and the incidence in males equals 1 in 100, then the expected incidence of affected homozygous females would be _______.\nChoices:\nA. 1 in 1000\nB. 1 in 4000\nC. 1 in 10 000\nD. 1 in 40 000\nAnswer:", " 1 in 40 000"], ["Question: Consanguinity shows a strong association with which pattern of inheritance?\nChoices:\nA. Autosomal dominant\nB. Autosomal recessive\nC. X-linked dominant\nD. X-linked recessive\nAnswer:", " Autosomal dominant"], ["Question: Consanguinity shows a strong association with which pattern of inheritance?\nChoices:\nA. Autosomal dominant\nB. Autosomal recessive\nC. X-linked dominant\nD. X-linked recessive\nAnswer:", " Autosomal recessive"], ["Question: Consanguinity shows a strong association with which pattern of inheritance?\nChoices:\nA. Autosomal dominant\nB. Autosomal recessive\nC. X-linked dominant\nD. X-linked recessive\nAnswer:", " X-linked dominant"], ["Question: Consanguinity shows a strong association with which pattern of inheritance?\nChoices:\nA. Autosomal dominant\nB. Autosomal recessive\nC. X-linked dominant\nD. X-linked recessive\nAnswer:", " X-linked recessive"], ["Question: Exon skipping is associated with:\nChoices:\nA. nonsense mutations.\nB. regulatory mutations.\nC. RNA processing mutations.\nD. silent mutations.\nAnswer:", " nonsense mutations."], ["Question: Exon skipping is associated with:\nChoices:\nA. nonsense mutations.\nB. regulatory mutations.\nC. RNA processing mutations.\nD. silent mutations.\nAnswer:", " regulatory mutations."], ["Question: Exon skipping is associated with:\nChoices:\nA. nonsense mutations.\nB. regulatory mutations.\nC. RNA processing mutations.\nD. silent mutations.\nAnswer:", " RNA processing mutations."], ["Question: Exon skipping is associated with:\nChoices:\nA. nonsense mutations.\nB. regulatory mutations.\nC. RNA processing mutations.\nD. silent mutations.\nAnswer:", " silent mutations."], ["Question: Simple tandem repeat polymorphisms in humans are most useful for\nChoices:\nA. solving criminal and paternity cases\nB. reconstructing the relationships of humans and chimps.\nC. estimating relationships of humans and Neanderthals\nD. transferring disease resistance factors into bone marrow cells\nAnswer:", " solving criminal and paternity cases"], ["Question: Simple tandem repeat polymorphisms in humans are most useful for\nChoices:\nA. solving criminal and paternity cases\nB. reconstructing the relationships of humans and chimps.\nC. estimating relationships of humans and Neanderthals\nD. transferring disease resistance factors into bone marrow cells\nAnswer:", " reconstructing the relationships of humans and chimps."], ["Question: Simple tandem repeat polymorphisms in humans are most useful for\nChoices:\nA. solving criminal and paternity cases\nB. reconstructing the relationships of humans and chimps.\nC. estimating relationships of humans and Neanderthals\nD. transferring disease resistance factors into bone marrow cells\nAnswer:", " estimating relationships of humans and Neanderthals"], ["Question: Simple tandem repeat polymorphisms in humans are most useful for\nChoices:\nA. solving criminal and paternity cases\nB. reconstructing the relationships of humans and chimps.\nC. estimating relationships of humans and Neanderthals\nD. transferring disease resistance factors into bone marrow cells\nAnswer:", " transferring disease resistance factors into bone marrow cells"], ["Question: Which of the following is a feature of X-linked dominant inheritance?\nChoices:\nA. Parental consanguinity\nB. Male to male transmission\nC. Transmission only by females\nD. Transmitted by males only to females\nAnswer:", " Parental consanguinity"], ["Question: Which of the following is a feature of X-linked dominant inheritance?\nChoices:\nA. Parental consanguinity\nB. Male to male transmission\nC. Transmission only by females\nD. Transmitted by males only to females\nAnswer:", " Male to male transmission"], ["Question: Which of the following is a feature of X-linked dominant inheritance?\nChoices:\nA. Parental consanguinity\nB. Male to male transmission\nC. Transmission only by females\nD. Transmitted by males only to females\nAnswer:", " Transmission only by females"], ["Question: Which of the following is a feature of X-linked dominant inheritance?\nChoices:\nA. Parental consanguinity\nB. Male to male transmission\nC. Transmission only by females\nD. Transmitted by males only to females\nAnswer:", " Transmitted by males only to females"], ["Question: Zinc finger proteins and helix-turn-helix proteins are\nChoices:\nA. types of DNA-binding proteins\nB. involved in the control of translation\nC. components of ribosomes\nD. part of the hemoglobin in blood cells\nAnswer:", " types of DNA-binding proteins"], ["Question: Zinc finger proteins and helix-turn-helix proteins are\nChoices:\nA. types of DNA-binding proteins\nB. involved in the control of translation\nC. components of ribosomes\nD. part of the hemoglobin in blood cells\nAnswer:", " involved in the control of translation"], ["Question: Zinc finger proteins and helix-turn-helix proteins are\nChoices:\nA. types of DNA-binding proteins\nB. involved in the control of translation\nC. components of ribosomes\nD. part of the hemoglobin in blood cells\nAnswer:", " components of ribosomes"], ["Question: Zinc finger proteins and helix-turn-helix proteins are\nChoices:\nA. types of DNA-binding proteins\nB. involved in the control of translation\nC. components of ribosomes\nD. part of the hemoglobin in blood cells\nAnswer:", " part of the hemoglobin in blood cells"], ["Question: Male breast cancer is associated with mutations in ___.\nChoices:\nA. BRCA1\nB. BRCA2\nC. NF1\nD. RET\nAnswer:", " BRCA1"], ["Question: Male breast cancer is associated with mutations in ___.\nChoices:\nA. BRCA1\nB. BRCA2\nC. NF1\nD. RET\nAnswer:", " BRCA2"], ["Question: Male breast cancer is associated with mutations in ___.\nChoices:\nA. BRCA1\nB. BRCA2\nC. NF1\nD. RET\nAnswer:", " NF1"], ["Question: Male breast cancer is associated with mutations in ___.\nChoices:\nA. BRCA1\nB. BRCA2\nC. NF1\nD. RET\nAnswer:", " RET"], ["Question: QTL analysis is used to\nChoices:\nA. identify chromosome regions associated with a complex trait in a genetic cross\nB. determine which genes are expressed at a developmental stage\nC. map genes in bacterial viruses\nD. identify RNA polymerase binding sites\nAnswer:", " identify chromosome regions associated with a complex trait in a genetic cross"], ["Question: QTL analysis is used to\nChoices:\nA. identify chromosome regions associated with a complex trait in a genetic cross\nB. determine which genes are expressed at a developmental stage\nC. map genes in bacterial viruses\nD. identify RNA polymerase binding sites\nAnswer:", " determine which genes are expressed at a developmental stage"], ["Question: QTL analysis is used to\nChoices:\nA. identify chromosome regions associated with a complex trait in a genetic cross\nB. determine which genes are expressed at a developmental stage\nC. map genes in bacterial viruses\nD. identify RNA polymerase binding sites\nAnswer:", " map genes in bacterial viruses"], ["Question: QTL analysis is used to\nChoices:\nA. identify chromosome regions associated with a complex trait in a genetic cross\nB. determine which genes are expressed at a developmental stage\nC. map genes in bacterial viruses\nD. identify RNA polymerase binding sites\nAnswer:", " identify RNA polymerase binding sites"], ["Question: Which component of transcribed RNA in eukaryotes is present in the initial transcript but is removed before translation occurs?\nChoices:\nA. Intron\nB. 3\u2019 Poly A tail\nC. Ribosome binding site\nD. 5\u2019 cap\nAnswer:", " Intron"], ["Question: Which component of transcribed RNA in eukaryotes is present in the initial transcript but is removed before translation occurs?\nChoices:\nA. Intron\nB. 3\u2019 Poly A tail\nC. Ribosome binding site\nD. 5\u2019 cap\nAnswer:", " 3\u2019 Poly A tail"], ["Question: Which component of transcribed RNA in eukaryotes is present in the initial transcript but is removed before translation occurs?\nChoices:\nA. Intron\nB. 3\u2019 Poly A tail\nC. Ribosome binding site\nD. 5\u2019 cap\nAnswer:", " Ribosome binding site"], ["Question: Which component of transcribed RNA in eukaryotes is present in the initial transcript but is removed before translation occurs?\nChoices:\nA. Intron\nB. 3\u2019 Poly A tail\nC. Ribosome binding site\nD. 5\u2019 cap\nAnswer:", " 5\u2019 cap"]]