TEST BANK
Genetics and Genomics in Nursing and Health Care
Theresa A. Beery, M. Linda Workman, and Julia A. Eggert
2nd Edition
www.Plusbay.Plus
,Table of Contents
Chapter 01 DNA Structure and Function 1
Chapter 02 Protein Synthesis 9
Chapter 03 Genetic Influence on Cell Division, Differentiation, and Gametogenesis 19
Chapter 04 Patterns of Inheritance 29
Chapter 05 Epigenetic Influences on Gene Expression 43
Chapter 06 Autosomal Inheritance and Disorders 47
Chapter 07 Sex Chromosome and Mitochondrial Inheritance and Disorders 55
Chapter 08 Family History and Pedigree Construction 61
Chapter 09 Congenital Anomalies, Basic Dysmorphology, and Genetic Assessment 68
Chapter 10 Enzyme and Collagen Disorders 74
Chapter 11 Common Childhood-Onset Genetic Disorders 84
Chapter 12 Common Adult-Onset Disorders 95
Chapter 13 Cardiovascular Disorders 103
Chapter 14 The Genetics of Cancer 110
Chapter 15 Genetic Contributions to Psychiatric and Behavioral Disorders 119
Chapter 16 Genetic and Genomic Testing 124
Chapter 17 Assessing Genomic Variation in Drug Response 129
Chapter 18 Health Professionals and Genomic Care 135
Chapter 19 Financial, Ethical, Legal, and Social Considerations 140
Chapter 20 Genetic and Genomic Variation 144
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, Test Bank - Genetics and Genomics in Nursing and Health Care, 2nd Edition (Beery, 2019)
Chapter 1: DNA Structure and Function
MULTIPLE CHOICE
1. In which body or cell area are most genes in humans located?
a. Nucleus
b. Mitochondrion
c. Cytoplasm
d. Plasma membrane
ANS: A
Most genes are part of the DNA located in the nucleus of body cells. Only a few genes are
located in a cell’s mitochondrion or mitochondria. There are no genes or DNA in either the
cytoplasm or the plasma membranes of any cell.
2. Which condition or statement exemplifies the concept of genomics rather than genetics?
a. The gene for insulin is located on chromosome 11 in all people.
b. Expression of any single gene is dependent on inheriting two alleles.
c. Sex-linked recessive disorders affect males more often than females.
d. One allele for each gene is inherited from the mother, and one is inherited from the
father.
ANS: A
Genetics is the study of the general mechanisms of heredity and the variation of inherited
traits. Genomics is the study of the function of all the nucleotide sequences present within
the entire genome of a s p e c i e s , Wi nWcW
l u.d iTn B
gSgeMn.
esWiS
n DNA coding regions and DNA noncoding
regions. Selections B, C, and D all refer to mechanisms of heredity. Only selection A refers
to the function of a specific nucleotide sequence.
3. What is the purpose of phosphorous in a DNA strand?
a. Linking the nucleotides into a strand
b. Holding complementary strands together
c. Ensuring that a purine is always paired with a pyrimidine
d. Preventing the separation of double-stranded DNA into single-stranded DNA
ANS: A
Each nucleoside becomes a complete nucleotide when a phosphate group is attached. The
phosphates have multiple binding sites, and each one can link to two nucleotides. These
linkages allow the nucleotides to be connected when placed into the DNA strand. The
nucleotides within each strand are held in position by the linked phosphate groups, which
act like the string holding a strand of beads together, forming a necklace.
4. What is the term used to define alternative forms of a gene that may result in different
expression of the trait coded for by that gene?
a. Alleles
b. Bases
c. Centromeres
d. Diploids
ANS: A
www.Plusbay.Plus 1|Page
Genetics and Genomics in Nursing and Health Care
Theresa A. Beery, M. Linda Workman, and Julia A. Eggert
2nd Edition
www.Plusbay.Plus
,Table of Contents
Chapter 01 DNA Structure and Function 1
Chapter 02 Protein Synthesis 9
Chapter 03 Genetic Influence on Cell Division, Differentiation, and Gametogenesis 19
Chapter 04 Patterns of Inheritance 29
Chapter 05 Epigenetic Influences on Gene Expression 43
Chapter 06 Autosomal Inheritance and Disorders 47
Chapter 07 Sex Chromosome and Mitochondrial Inheritance and Disorders 55
Chapter 08 Family History and Pedigree Construction 61
Chapter 09 Congenital Anomalies, Basic Dysmorphology, and Genetic Assessment 68
Chapter 10 Enzyme and Collagen Disorders 74
Chapter 11 Common Childhood-Onset Genetic Disorders 84
Chapter 12 Common Adult-Onset Disorders 95
Chapter 13 Cardiovascular Disorders 103
Chapter 14 The Genetics of Cancer 110
Chapter 15 Genetic Contributions to Psychiatric and Behavioral Disorders 119
Chapter 16 Genetic and Genomic Testing 124
Chapter 17 Assessing Genomic Variation in Drug Response 129
Chapter 18 Health Professionals and Genomic Care 135
Chapter 19 Financial, Ethical, Legal, and Social Considerations 140
Chapter 20 Genetic and Genomic Variation 144
,www.Plusbay.Plus
, Test Bank - Genetics and Genomics in Nursing and Health Care, 2nd Edition (Beery, 2019)
Chapter 1: DNA Structure and Function
MULTIPLE CHOICE
1. In which body or cell area are most genes in humans located?
a. Nucleus
b. Mitochondrion
c. Cytoplasm
d. Plasma membrane
ANS: A
Most genes are part of the DNA located in the nucleus of body cells. Only a few genes are
located in a cell’s mitochondrion or mitochondria. There are no genes or DNA in either the
cytoplasm or the plasma membranes of any cell.
2. Which condition or statement exemplifies the concept of genomics rather than genetics?
a. The gene for insulin is located on chromosome 11 in all people.
b. Expression of any single gene is dependent on inheriting two alleles.
c. Sex-linked recessive disorders affect males more often than females.
d. One allele for each gene is inherited from the mother, and one is inherited from the
father.
ANS: A
Genetics is the study of the general mechanisms of heredity and the variation of inherited
traits. Genomics is the study of the function of all the nucleotide sequences present within
the entire genome of a s p e c i e s , Wi nWcW
l u.d iTn B
gSgeMn.
esWiS
n DNA coding regions and DNA noncoding
regions. Selections B, C, and D all refer to mechanisms of heredity. Only selection A refers
to the function of a specific nucleotide sequence.
3. What is the purpose of phosphorous in a DNA strand?
a. Linking the nucleotides into a strand
b. Holding complementary strands together
c. Ensuring that a purine is always paired with a pyrimidine
d. Preventing the separation of double-stranded DNA into single-stranded DNA
ANS: A
Each nucleoside becomes a complete nucleotide when a phosphate group is attached. The
phosphates have multiple binding sites, and each one can link to two nucleotides. These
linkages allow the nucleotides to be connected when placed into the DNA strand. The
nucleotides within each strand are held in position by the linked phosphate groups, which
act like the string holding a strand of beads together, forming a necklace.
4. What is the term used to define alternative forms of a gene that may result in different
expression of the trait coded for by that gene?
a. Alleles
b. Bases
c. Centromeres
d. Diploids
ANS: A
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