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alleles
amniocentesis
aneuploidy
barr body
carrier
chorionic villus sampling cvs
codominance
cystic fibrosis
cytological maps
deletion
down syndrome
duchenne muscular dystrophy
duplication
epistasis
fragile x syndrome
genetic map
genetic recombination
genomic imprinting
hemophilia
huntington's disease
hybridization
incomplete dominance
inversion
linked gene
monosomic
mosaic
nondisjuction
pedigree
pleiotropy
polygenic inheritance
polyploidy
recombinant
sex linked gene
sickle-cell disease
tay-sachs disease
translocation
trisomic
true-breeding
wild type