16.
A mutation in which a nucleotide or a codon
in DNA is replaced with a different nucleotide
17.
mutation that shifts the "reading" frame of
the genetic message by inserting or deleting
a nucleotide
18.
a mutation in which one or more nucleotides
are added to a gene
19.
A diagram that shows the occurrence of a
genetic trait in several generations of a family
20.
an inactive substance that is a vehicle for a
radioactive tracer of the same substance and
that assists in its recovery after some
chemical reaction
25.
situation in which both alleles of a gene
contribute to the phenotype of the organism
26.
one allele is not completely dominant over
the other allele
27.
an autosomal trait that is influenced by the
presence of male or female sex hormones
28.
A human genetic disease caused by a
dominant allele; characterized by
uncontrollable body movements and
degeneration of the nervous system; usually
fatal 10 to 20 years after the onset of
symptoms.
29.
Technique that allows a physician to remove
from the amnion, the sac that surrounds the
fetus, between the 14th and 16th week of
pregnancy
30.
Sampling of cells derived from the zygote
that grow between the mother's uterus and
placenta between the 8th and 10th week of
pregnancy