Ch. 2 Vocab Flashcards
23 matching pairs of rod-shaped structures located in the nucleus
chromosomes
a complex molecule shaped like a twisted ladder or staircase
deoxyribonucleic acid (DNA)
the blueprint for creating all of the traits that organisms carry
genes
the process which DNA replicates itself, permitting the duplication of chromosomes and ultimately the formation of new cells with identical genetic material
mitosis
how sex cells reproduce; like mitosis but chromosomes complete “crossing over”
meiosis
the cells of sexual reproduction; sperm (in males) and ova (in females)
gametes
fertilized egg
zygote
ovary
ovum
when more than one ovum is released and each is fertilized by two different sperm; fraternal twins
dizygotic (DZ) twins
occurs when zygote splits into two distinct separate but identical zygotes; shares same genotype with identical instructions for all physical and psychological characteristics; identical twins
monozygotic (MZ) twins
chromosomes expressed in different forms that influence a variety of physical characteristics
alleles
when alleles of the pair of chromosomes are alike with regard to a specific characteristic
homozygous
when alleles of the pair of chromosomes are different with regard to a specific characteristic
heterozygous
when some genes that are passed through are always expressed regardless of the gene they are paired with while other genes will be expressed only if paired with another recessive gene
dominant-recessive inheritance
when an individual is heterozygous for a particular trait and the dominant trait is expressed, this individual becomes a
carrier
genetic inheritance pattern in which both genes influence the characteristic
incomplete dominance
causes red blood cells to become crescent, or sickle, shaped; about 5% of African Americans newborns carry this recessive trait
sickle cell trait
most traits are a function of the interaction of many genes
polygenic inheritance
refers to the instance in which the expression of a gene is determined by whether it is inherited from the mother or the father
genomic imprinting
a common recessive disorder that prevents the body from producing an enzyme that breaks down phenylalanine (an amino acid) from proteins
phenylketonuria (PKU)
a dominant-recessive disorder carried on the X chromosome; an intellectual disability
Fragile X syndrome
a condition in which the blood does not clot normally; a recessive disease inherited through genes on the X chromosomes
hemophilia
most widely known chromosome disorder; trisomy 21; an extra chromosome; occurs in about 1/1500 births
down syndrom
males are born with an extra X chromosome
Klinefelter syndrome