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2.2 & 2.3 Vocab Term
Question | Answer |
---|---|
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 |