Exam 4: Pedigree Analysis in Human Genetics
Exam 1: A Perspective on Human Genetics60 Questions
Exam 2: Cells and Cell Division60 Questions
Exam 3: Transmission of Genes from Generation to Generation60 Questions
Exam 4: Pedigree Analysis in Human Genetics60 Questions
Exam 5: The Inheritance of Complex Traits60 Questions
Exam 6: Cytogenetics - Karyotypes and Chromosome Aberrations60 Questions
Exam 7: Development and Sex Determination60 Questions
Exam 8: The Structure - Replication - and Chromosomal Organization of DNA60 Questions
Exam 9: Gene Expression and Gene Regulation60 Questions
Exam 10: From Proteins to Phenotypes60 Questions
Exam 11: Genome Alterations - Mutation and Epigenetics60 Questions
Exam 12: Genes and Cancer60 Questions
Exam 13: An Introduction to Genetic Technology60 Questions
Exam 14: Biotechnology and Society60 Questions
Exam 15: Genomes and Genomics60 Questions
Exam 16: Reproductive Technology - Genetic Testing - and Gene Therapy60 Questions
Exam 17: Genes and The Immune System60 Questions
Exam 18: Genetics of Behavior60 Questions
Exam 19: Population Genetics and Human Evolution60 Questions
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Individuals with Marfan syndrome experience an eyesight problem called ____________________.
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(Short Answer)
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nearsightedness
The variable phenotypic expression shown in camptodactyly results from the interaction of ____________________ and ________________factors.
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genetic; nongenetic
nongenetic; genetic
genetic; environmental
environmental; genetic
The chance of a child having albinism when both of his parents are heterozygous for the disorder is ____ percent.
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(Multiple Choice)
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Correct Answer:
B
Cytoplasmic organelles that convert energy from food molecules in ATP and are transmitted from mothers to all their children through the cytoplasm of the egg are called ____________________.
(Short Answer)
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If a man expresses an X-linked recessive trait,his ____________________ was either homozygous or heterozygous for the trait.
(Short Answer)
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Genetic diseases transmitted only by a mother to both sons and daughters result from ____________________ genes.
(Short Answer)
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A trait shows ____ if the phenotype of that trait is present in less than 100% of those with the related genotype.
(Multiple Choice)
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If a pedigree analysis suggests that an autosomal or X-linked inheritance pattern is equally likely,then additional genetic testing is needed to identify the pattern of inheritance.
(True/False)
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Mitochondrial gene defects most often affect the ____________________ and the ____________________.
(Short Answer)
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The frequency of heterozygotes for cystic fibrosis shows ethnic variations.
(True/False)
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The gene responsible for Marfan syndrome encodes a protein associated with ____.
(Multiple Choice)
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A marriage between two related individuals,such as first cousins,is called ____________________.
(Short Answer)
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A pedigree is always able to provide enough information to rule out all but one possible pattern of inheritance.
(True/False)
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The probability that a disease phenotype will appear when a disease-related genotype is present is called ____________________.
(Short Answer)
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The basic method of genetic analysis in humans requires a(n)____________________ of several generations.
(Short Answer)
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One characteristic of an autosomal dominant trait is that ____.
(Multiple Choice)
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Most of those affected with an autosomal dominant genetic disorder are homozygous for that trait.
(True/False)
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When affected males produce all affected daughters and no affected sons,the pattern of inheritance is likely to be ____________________.
(Short Answer)
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