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gene (K)
a segment of DNA on a chromosome
allele (P)
an alternative version of a gene that will produce a different phenotype
genetic disorder (E)
an abnormal condition that a person inherits through genes or chromosomes
phenotype (L)
an organism’s observable physical or physiological traits
codominance (A)
the phenotypes of both alleles are exhibited in the heterozygote
karyotype (S)
a picture of all the chromosomes in a cell arranged in pairs by their size and shape
law of independent assortment (G)
mendelian principle stating that genes for different traits are inherited independently of each other
recessive allele (H)
an allele whose phenotypic expression is not observed in a heterozygote
genetics (R)
the scientific study of heredity
traits (D)
one (or more) characteristic(s) that an organism can pass on to its offspring
homozygous (B)
having two identical alleles for a given gene
probability (I)
the likelihood that a particular event will occur
meiosis (O)
cell division that occurs in gametes and results in the formation of haploid sex cells after two divisions
Sex-Linked Gene (N)
a gene that is carreid on the X or Y chromosome
law of segregation (C)
mendelian principle stating that the two alleles in a pair are separated into different gametes during meiosis
nondisjunction (J)
an error that can occur during cell division, where homologous chromosomes fail to separate properly
pedigree (M)
a chart or family tree that tracks which members of a family carry a particular trait
mutation (F)
a change in the DNA sequence of a gene
Punnett square (Q)
a chart that shows all the possible combinations of alleles that can result from a genetic cross
genotype (T)
an organism’s genetic makeup or allele combinations