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Complete Test Bank for Genetics and Genomics in Nursing and Health Care, 2nd Edition – Theresa A. Beery, M. Linda Workman, Julia A. Eggert

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This resource is the full Test Bank for the Second Edition of "Genetics and Genomics in Nursing and Health Care" by Theresa A. Beery, M. Linda Workman, and Julia A. Eggert (2018). It features a robust collection of Multiple Choice questions accompanied by a detailed Answer Section that provides the correct choices and identifies the relevant concepts for each question. The material spans 20 comprehensive chapters, covering foundational and advanced nursing genetics topics such as DNA Structure and Function, Protein Synthesis, and Epigenetic Influences on Gene Expression. It provides evaluated content on Patterns of Inheritance, including autosomal dominant, autosomal recessive, and X-linked transmission, as well as complex multifactorial disorders. Students can practice identifying pedigree symbols, assessing congenital anomalies, and understanding dysmorphology. Detailed questions address specific health conditions like Sickle Cell Disease, Cystic Fibrosis, Duchenne Muscular Dystrophy, Hemophilia, Huntington Disease, and Hereditary Hemochromatosis. Additionally, the test bank covers critical clinical areas including Pharmacogenetics, Genetics of Cancer, Psychiatric and Behavioral Disorders, and the Financial, Ethical, Legal, and Social Considerations of genomic care. This is an essential study tool for mastering genomic variation and its application in modern nursing practice.

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TEST BANK
V

GeneticsVandVGenomicsVinVNursingVandVHealthVCare

byVTheresaVA.VBeery,VM.VLindaVWorkman
SecondVEdition




FULL TEST BANK!!!
V V

, ChapterV1:VDNAVStructureVandVFunction

MultipleVChoice
IdentifyVtheVchoiceVthatVbestVcompletesVtheVstatementVorVanswersVtheVquestion.

VV A. 1.V InVwhichVbodyVorVcellVareaVareVmostVgenesVinVhumansVlocated?
A. Nucleus
B. Mitochondrion
C. Cytoplasm
D. PlasmaVmembrane

VV A. 2.V WhichVconditionVorVstatementVexemplifiesVtheVconceptVofVgenomicsVratherVthanVgenetics?
A. TheVgeneVforVinsulinVisVlocatedVonVchromosomeV11VinVallVpeople.
B. ExpressionVofVanyVsingleVgeneVisVdependentVonVinheritingVtwoValleles.
C. Sex-linkedVrecessiveVdisordersVaffectVmalesVmoreVoftenVthanVfemales.
D. OneValleleVforVeachVgeneVisVinheritedVfromVtheVmother,VandVoneVisVinheritedVf
romVtheVfather.
VV A. 3.V WhatVisVtheVpurposeVofVphosphorousVinVaVDNAVstrand?
A. LinkingVtheVnucleotidesVintoVaVstrand
B. HoldingVcomplementaryVstrandsVtogether
C. EnsuringVthatVaVpurineVisValwaysVpairedVwithVaVpyrimidine
D. PreventingVtheVseparationVofVdouble-strandedVDNAVintoVsingle-strandedVDNA

V A.
4.VWhatVisVtheVtermVusedVtoVdefineValternativeVformsVofVaVgeneVthatVmayVresultVin
VdifferentVexpressionVofVtheVtraitVcodedVforVbyVthatVgene?
A. Alleles
B. Bases
C. Centromeres
D. Diploids
V D. 5.VWhatVpercentageVofVbasesVinVaVstretchVofVdouble-
strandedVDNAVthatVcontainsV30%VguanineV(G)VbasesVwouldVbeVadenineV(A)?
A. 70%
B. 60%
C. 30%
D. 20%

V C.
6.VWhatVisVtheVtermVusedVtoVdescribeVtheVorganizedVpictureVofVtheVpairedVchromo
somesVwithinVaVcellVusedVtoVdetermineVwhetherVchromosomeVnumbers,Vstructures,VandVba
ndingVpatternsVareVnormal?
A. Pedigree
B. Phenotype
C. Karyotype
D. Autotype

V D.
7.VWhatVwouldVbeVtheVsequenceVofVDNAVthatVisVcomplementaryVtoVaVDNAVs
ectionVwithVtheVbaseVsequenceVofVGGTCAATCCTTAG?
A. GATTCCTAACTGG
B. TTGACCGAAGGCT
C. AACTGGCTTCCGA
D. CCAGTTAGGAATC

,VV B. 8.V WhichVofVtheseVcomplementaryVbaseVpairsVformVtheVstrongestVorV“tightest”Vassociation?
A. AdenineVandVthymine
B. CytosineVandVguanine
C. GuanineVandVthymine
D. CytosineVandVadenine

VV A 9.V WhatVactivityVoccursVduringVMVphaseVofVtheVcellVcycle?
A. TheVcellVundergoesVcytokinesis.
B. ActivityVstops,VandVtheVcellV“sleeps.”
C. AllVDNAVisVcompletelyVreplicated.
D. TheVcellVgreatlyVincreasesVproteinVsynthesis.

VV B.V V 10.V WhichVchromosomeVnumberVrepresentsVtheVeuploidVstateVforVnormalVhumanVsomaticVcells?
A. 44
B. 46
C. 47
D. 48

VV A.V 11.V HowVdoesVtheVproteomeVdifferVfromVtheVgenome?
A. TheVproteomeVchangesVinVresponseVtoVintracellularVandVextracellularVsignals.
B. TheVgenomeVchangesVinVresponseVtoVintracellularVandVextracellularVsignals.
C. TheVproteomeVisVstableVinVsomaticVcellsVandVunstableVinVgermVcells,Vwher
easVtheVgenomeVisVstableVinVbothVsomaticVcellsVandVgermVcells.
D. TheVgenomeVisVstableVinVsomaticVcellsVandVunstableVinVgermVcells,Vwher
easVtheVproteomeVisVstableVinVbothVsomaticVcellsVandVgermVcells.
VV C.V V 12.V WhatVisVtheVmostVoutstandingVfeatureVofVaVmatureVhaploidVcell?
A. ItVisVusuallyVhomozygous.
B. TheVsexVchromosomesVareVmissing.
C. OnlyVoneVchromosomeVofVeachVpairVisVpresent.
D. DNAVsynthesisVoccursVafterVmitosisVinsteadVofVbefore.

VV D.V V 13.V AtVwhatVphaseVofVtheVcellVcycleVareVchromosomesVvisibleVasVseparateVstructures?
A. G1
B. G2
C. S
D. M
VV B.V 14.V WhichVstatementVaboutVtheVcellVcycleVphaseVofVG0V isVtrue?
A. HyperplasticVgrowthVinVplaceVofVhypertrophicVgrowth
B. PerformanceVofVspecificVdifferentiatedVfunctions
C. InitiationVandVcompletionVofVnucleokinesis
D. ReplicationVofVDNA

VV B.V 15.V WhatVisVtheVresultVofVnormalVDNAVreplication?
A. FormationVofVtwoVnewVdaughterVcells
B. FormationVofVtwoVidenticalVsetsVofVDNA
C. DisappearanceVofVtheVoriginalVparentVcell
D. ActivationVandVattachmentVofVspindleVfibers

, VV A.V 16.V WhichVstatementVregardingVchromosomeVstructureVorVfunctionVisVtrue?
A. TheVchromatidsVofVanyVsingleVchromosomeVareVknownVasV“sisterVchromatids.”
B. TheVgenesVlocatedVonVtheVtelomeresVofVchromosomesVareVidenticalVtoVtheVg
enesVinVtheVcentromeres.
C. ImmediatelyVbeforeVtheVmitosisVphaseVofVcellVdivision,VtheVchromosomes
VofVallVsomaticVcellsVareVhaploid.
D. AVspecificVgeneValleleVonVoneVchromosomeVhasVaVcomplementaryValleleVonVth
eVotherVchromosomeVofVaVpair.
VV C.V V 17.V WhyVdoesVaVpersonVwithVnormalVchromosomesVonlyVhaveVtwoVallelesVforVanyVsingleVgeneVtrait?
A. AVminimumVofVtwoVallelesVisVrequiredVforVtheVexpressionVofVmonogenicVtraits.
B. WhenVaVdominantValleleVisVpairedVwithVaVrecessiveVallele,VonlyVtheVdominantV
alleleVisVexpressed,VandVtheVrecessiveValleleVisVsilent.
C. OneValleleVforVtheVmonogenicVtraitVisVonVtheVpaternallyVderivedVchromoso
me,VandVtheVotherValleleVisVonVtheVmaternallyVderivedVchromosome.
D. ExpressionVofVmoreVthanVtwoVallelesVofVanyVsingle-
geneVtraitVresultsVinVenhancedVexpressionVofVrecessiveVallelesVandVsuppress
edVexpressionVofVdominantValleles.
VV C 18.V UnderVwhatVnormalVconditionVareVgenotypeVandVphenotypeValwaysVtheVsame?
A. EuploidyVofValleles
B. AneuploidyVofValleles
C. HomozygosityVofValleles
D. HeterozygosityVofValleles

V V D.V 19.V WhatVwouldVbeVtheVexpectedVresultVofVaVdrugVthatVaffectedVaVparticularVtissueVbyVcaus
ingVnewVDNAVtoVformVwithVcovalentVbondsVinsteadVofVhydrogenVbonds?
A. NoneVofVtheVcellsVinVtheVaffectedVtissueVwouldVbeVableVtoVleaveVG0V andVente
rVtheVcellVcycle.
B. ReplicationVofVDNAVwouldVresultVinVidenticalVDNAVstrandsVinste
adVofVcomplementaryVstrands.
C. MitosisVofVcellsVinVtheVtissueVwouldVresultVinVtheVproductionVofVthreeVnewV
daughterVcellsVinsteadVofVjustVtwo.
D. TheVnewVcellsVthatVformedVwithinVthisVtissueVwouldVnotVbeVableVtoVcompleteV
theVnextVroundVofVmitosisVsuccessfully.
VV B.V 20.V HowVdoesVtheVDNAVenzymeVtopoisomeraseVcontributeVtoVDNAVreplication?
A. UnwindsVtheVdoubleVhelixVandVseparatesVtheVdouble-strandedVDNA
B. CreatesVaV“nick”VinVtheVDNAVsupercoils,VallowingVthemVtoVstraightenV
beforeVreplication
C. InitiatesVDNAVsynthesisVinVmultipleVsitesVdownVtheVstrand,VmakingVtheVproces
sVmoreVefficient
D. ConnectsVandVlinksVtheVindividualVpiecesVofVnewlyVsynthesizedVDNAVtoV
formVaVsingleVstrand
VV A.V 21.V WhereVisVtelomericVDNAVlocated?
A. AtVtheVtipsVofVtheVpVandVqVarmsVofVchromosomes.
B. InVtheVmitochondriaVofVallVsomaticVcells
C. OnlyVinVtheVgermVcellsV(ovaVandVsperm)
D. WithinVtheVhistonesVofVtheVsolenoid

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