Exam 4: Pedigree Analysis in Human Genetics

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The main problem for sufferers of cystic fibrosis is

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C

The gene responsible for Marfan syndrome encodes a protein associated with

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B

Which of the following is NOT a symptom of Marfan syndrome?

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D

The analysis of a pedigree is complete when the information in the pedigree supports the hypothesis formed by the geneticist.

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Which of the following is NOT a characteristic of an autosomal recessive trait?

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Mendel's laws apply to all sexually reproducing organisms. Therefore, the basic methods of genetic analysis in humans and other organisms is the same.

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Human traits are controlled only by the genetic material found in the 46 chromosomes.

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Color blindness only occurs in males.

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Two phenotypically normal parents have six children. Two daughters and two sons have the same genetic disease. This would be the expected situation for

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How would you distinguish between a trait that is X-linked dominant trait and one that is autosomal dominant?

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Approximately how many Y-linked genes have been discovered?

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Mitochondrial gene defects mainly cause myopathies (conditions affecting ____________________), and encephalomyopathies (conditions also affecting ____________________).

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The gene that codes for the connective tissue protein fibrillin is the gene that causes ____________________.

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Valeria has a serious disorder called fragile X syndrome and her brother does not have the disorder. Her mother does not have the disorder but her father does. What is the most likely inheritance pattern for fragile X syndrome?

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Adults who have children who have died from lethal recessive disorders are most likely ____________________.

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A defective form of the protein dystrophin is involved in the diseases __________ and ________.

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Is it easier to work out pedigrees for dominant traits than for recessive ones? What can complicate the analysis of dominant traits?

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The underlying problem with cystic fibrosis is

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Duchenne muscular dystrophy and Becker's muscular dystrophy represent allelic forms of the same X-linked gene.

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Hemophilia was a significant issue in the life of

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