Monohybrid cross
A cross between two organisms that are heterozygous for the character being followed
hybridization
in genetics, the mating or crossing of two-breeding varieties
Punnet square
A diagram used in the study of inheritance to show the predicted genotypic results of a random fertilization in genetic crosses between individuals of known genotype
alleles
any of the alternative versions of a gene that may produce distinguishable phenotypic effects
Dihybrids
An organism that is heterozygous with respect to two genes of interest.
Dominant allele
An allele that is fully expressed in a phenotype or heterozygous
P generation
true breeding parent individuals from which F1 hybrid offspring are derived in studies of inheritance
carriers
an individual who is heterozygous at a given genetic locus for a recessively inherited disorder
Trait
one or two or more detectable variants in a genetic character
pleiotropy
the ability of a single gene to have multiple effects
Huntington’s disease
a disease caused by dominant allele; uncontrolled body movements; usually fatal 10 to 20 years after the onset of symptoms.
cystic fibrosis
A human genetic disease by a reccesive allele for chloride channel protein; infection
multiplication rule
a rule stating that the probability of two or more independent events occurring together can be determined by multiplying their individual probabilities.
Complete dominance
Dominate fully shows
Epistasis
One gene affects another
Interaction
Aminocentesis
A technique associated with prenatal diagnosis
Amniotic fluid is obtained by aspiration from a needle inserted into the uterus
Law of independent assortment
Second law
Chrionic villus sampling
A technique associated in which a sample sample of the fetal portion of the placenta ta is removed for analysis
Test cross
Breeding an organism of unknown genotype with a homozygous recessive Indian to determine the unknown genotype.
Quantitative charcters
A heritable feature that varies continuously over a range rather than in an either or fashion
Tay sach disease
A human genetic disease caused by a recessive allele for a dysfunctional enzyme
Phenotype
The physical traits of an organism
Law of segregation
First law
Homozygote
An organism that has a pair of identical alleles for a gene