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2.2 & 2.3 Vocab Term

QuestionAnswer
alleles
autosomes
benign
base pair
centromere
chromatid
chromosome
deletion mutation
DNA
dominant allele
eukaryotic
Familial Hypercholesterolemia
frameshift mutation
gene
genome
genotype
gestational diabetes
heterozygous
homologous chromosomes
homozygous
insertion mutation
karyotype
magnetic resonance imaging (MRI)
malignant
meiosis
messenger RNA (mRNA)
metastasis
mitosis
mutation
Nondisjunction
nucleotides
pedigree
phenotype
plan of care
point mutation
polymerase chain reaction
prognosis
protein
protein synthesis
punnett square
recessive allele
restriction enzyme
ribonucleic acid (RNA)
rRNA
sex chromosomes
silent mutation
transcription
translation
tRNA
ultrasound imaging
Created by: user-1719944
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