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62 Cards in this Set

  • Front
  • Back

niche-picking

process of deliberately seeking environments that are compatible with one’s genetic makeup

amniocentesis

prenatal diagnostic technique that uses a syringe to withdraw a sample of amniotic fluid through the mother’s abdomen

homozygous

when the alleles in a pair of chromosomes are the same

amniotic fluid

fluid that surrounds the fetus

infant mortality

the number of infants out of 1,000 births who die before their first birthday

spina bifida

disorder in which the embryo’s neural tube does not close properly

hypoxia

a birth complication in which umbilical blood flow is disrupted and the infant does not receive adequate oxygen

cerebral cortex

wrinkled surface of the brain that regulates many functions that are distinctly human

cesarean section

surgical removal of an infant from the uterus through an incision made in the mother’s abdomen

monozygotic twins

the result of a single fertilized egg splitting to form two new individuals; also called identical twins

autosomes

first 22 pairs of chromosomes

teratogen

an agent that causes abnormal prenatal development

extremely low birth weight

newborns who weigh less than 1,000 grams (2.2 pounds)

amnion

inner sac in which the developing child rests

nonshared environmental influences

forces within a family that make siblings different from one another

heterozygous

when the alleles in a pair of chromosomes differ from each other

cephalocaudal principle

a principle of physical growth that states that structures nearest the head develop first

dizygotic twins

the result of two separate eggs fertilized by two sperm; also called fraternal twins

genotype

person's hereditary makeup

incomplete dominance

situation in which one allele does not dominate another completely

very low birth weight

newborns who weigh less than 1,500 grams (3.3 pounds)

stress

physical and psychological responses to threatening or challenging conditions

embryo

term given to the zygote once it is completely embedded in the uterine wall

age of viability

age at which a fetus can survive outside the womb because most of its bodily systems function adequately; typically at seven months after conception

phenylketonuria (PKU)

inherited disorder in which the infant lacks a liver enzyme

ectoderm

outer layer of the embryo, which becomes the hair, outer layer of skin, and nervous system

germ disc

small cluster of cells near the center of the zygote that eventually develop into the baby

dominant

Form of an allele whose chemical instructions are followed

in vitro fertilization

process by which sperm and an egg are mixed in a petri dish to create a zygote, which is then placed in a woman’s uterus

fetal alcohol spectrum disorder

disorder affecting babies whose mothers consumed large amounts of alcohol while they were pregnant

ultrasound

prenatal diagnostic technique that uses sound waves to generate an image of the fetus

chromosomes

threadlike structures in the nuclei of cells that contain genetic material

mesoderm

middle layer of the embryo, which becomes the muscles, bones, and circulatory system

period of the fetus

longest period of prenatal development, extending from the 9th until the 38th week after conception

proximodistal principle

principle of physical growth that states that structures nearest the center of the body develop first

zygote

fertilized egg

Behavioral genetics

the branch of genetics that studies the inheritance of behavioral and psychological traits

chorionic villus sampling

prenatal diagnostic technique that involves taking a sample of tissue from the placenta

sex chromosomes

23rd pair of chromosomes; these determine the sex of the child

prenatal development

the many changes that turn a fertilized egg into a newborn human

gene

group of nucleotide bases that provides a specific set of biochemical instructions

low birth weight

newborns who weigh less than 2,500 grams (5.5 pounds)

preterm or premature

babies born before the 36th week after conception

sickle-cell trait

disorder in which individuals show signs of mild anemia only when they are seriously deprived of oxygen; occurs in individuals who have one dominant allele for normal blood cells and one recessive sickle-cell allele

phenotype

physical, behavioral, and psychological features that result from the interaction between one's genes and the environment

crowning

appearance of the top of the baby’s head during labor

endoderm

inner layer of the embryo, which becomes the lungs and digestive system

alleles

variations of genes

fetal medicine

field of medicine concerned with treating prenatal problems before birth

polygenic inheritance

when phenotypes are the result of the combined activity of many separate genes

Vernix

substance that protects the fetus’s skin during development

heritability coefficient

a measure (derived from a correlation coefficient) of the extent to which a trait or characteristic is inherited

recessive

allele whose instructions are ignored in the presence of a dominant allele

Huntington’s disease

progressive and fatal type of dementia caused by dominant alleles

placenta

structure through which nutrients and wastes are exchanged between the mother and the developing child

eugenics

effort to improve the human species by letting only people whose characteristics are valued by a society mate and pass along their genes

implantation

step in which the zygote burrows into the uterine wall and establishes connections with the woman’s blood vessels

umbilical cord

structure containing veins and arteries that connects the developing child to the placenta

deoxyribonucleic acid

molecule composed of four nucleotide bases that is the biochemical basis of heredity

cesarean section (C-section)

surgical removal of an infant from the uterus through an incision made in the mother’s abdomen

deoxyribonucleic acid (DNA)

molecule composed of four nucleotide bases that is the biochemical basis of heredity

preterm (premature)

babies born before the 36th week after conception