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2.6: Key Terms

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    233462
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    active genotype-environment correlation
    event in which individuals select particular environments or experiences based on their genotype
    age of viability
    age at which a fetus born prematurely (before the thirty-seventh week of pregnancy) may have a chance of survival outside the womb, usually with intensive medical intervention
    allele
    variant of a gene
    amniocentesis
    test in which a needle is inserted through the mother’s abdomen to take a sample of the amniotic fluid and look for chromosomal disorders and some types of genetic defects
    Apgar test
    test administered to a newborn one minute after delivery and again at five minutes after delivery to assess their condition after birth; detects major abnormalities
    attachment
    the emotional connection a child feels toward their caregiver based on consistency and quality of care
    autosome
    chromosome in the nucleus that is not a sex chromosome
    behavioral genetics
    interdisciplinary field that focuses on the study of heredity-behavior relationships
    blastocyst
    small cluster of a few hundred cells formed shortly after conception
    bonding
    one-way relationship consisting of a caregiver’s emotional connection to the infant
    cephalocaudal growth
    growth that occurs from head to feet, allowing a fetus to grow longer
    cesarean birth
    medical procedure in which a doctor makes an incision in a birth mother’s abdomen and uterus to deliver the fetus and placenta
    chorionic villus sampling
    prenatal test that uses a placental tissue sample to determine whether chromosomal or genetic disorders are present in the fetus
    chromosomal disorder
    condition that occurs with an incorrect number of chromosomes or results from structural abnormalities of the chromosome
    chromosome
    strand of the DNA sequence in the nucleus of an individual’s cells that carries genes transmitting hereditary information
    codominant trait
    characteristic observed when two different alleles are expressed at the same time
    conception
    union of sperm and ovum (egg)
    congenital disorder
    any abnormality present at birth
    contraception
    method used to reduce chances of conception
    dizygotic twins
    (or fraternal) twins that occur when two ova are fertilized at the same time
    DNA (also, deoxyribonucleic acid)
    molecule that contains an individual’s genetic information
    DNA methylation
    process whereby methyl groups are added to or removed from DNA, potentially causing changes in gene expression
    dominant trait
    characteristic observed when only one copy of the allele is needed to express a phenotype
    embryonic period
    second developmental period of pregnancy, during which the blastocyst becomes an embryo and organogenesis begins
    evocative (or reactive) genotype-environment correlation
    event in which an individual’s genetically influenced traits elicit an environmental response
    failure to thrive
    situation in which a premature infant’s height and weight are below the third percentile
    fallopian tube
    part of the female reproductive system where egg is released and through which it travels to reach the uterus
    fetal period
    last developmental period of pregnancy, during which the fetus grows quickly
    gamete
    sex cell, the ovum or sperm, that carries twenty-three chromosomes
    gene
    hereditary unit composed of a specific DNA sequence that occupies a specific location along a chromosome in an individual
    genome
    complete sequence of an organism’s DNA
    genotype
    individual’s particular genetic composition of alleles at specific locations
    genotype × environment interaction
    event that occurs when the expression of a genotype depends on the environment
    germinal period
    first developmental period of pregnancy, when conception occurs and the blastocyst travels through the fallopian tubes to the uterus
    heterozygous
    trait in which an individual receives different alleles from each biological parent for a given trait
    homozygous
    trait in which an individual receives identical alleles from each biological parent for a given trait
    hormone
    chemical released by glands that controls and regulates bodily functions
    implantation
    process in which a blastocyst embeds within the uterus
    in vitro fertilization (IVF)
    form of assisted reproductive technology (ART) in which a fertilized egg is transferred into a uterus for implantation
    incomplete dominance
    form of genetic expression in which both inherited alleles are partially expressed
    infertility
    inability to successfully conceive after one year of trying
    low birth weight
    birth weight less than 5 lb 8 oz
    mass-to-specific growth
    growth in which large movements and structures develop before smaller or more specified movements and structures
    meiosis
    type of cell division that occurs during gamete production and results in their containing only one member of each chromosome pair
    mitosis
    type of cell division in which a cell duplicates itself and its DNA
    monozygotic twins
    (or identical) twins that occur when a zygote splits into two clusters of cells, creating two genetically identical zygotes
    multifactorial inheritance
    phenotype resulting from multiple genetic and environmental factors
    natural childbirth
    a childbirth method using nonpharmaceutical techniques to help minimize pain and the need for medical intervention for the birth mother
    neonatal behavioral assessment scale (NBAS)
    test assessing a newborn’s neurological and physical health, typically given three to four days after birth
    organogenesis
    the formation of organs during the embryonic period
    ovary
    part of the female reproductive system that releases eggs (ova)
    oxytocin
    hormone that helps initiate labor and plays a role in forming bonds with others
    parental leave
    policies that allow parents to take time off work, often paid, to care for a newborn for a period of time
    passive genotype-environment correlation
    event that occurs when parents provide offspring with both genes and environment
    phenotype
    observable expression of someone’s genome
    placenta
    a temporary organ connecting the uterus to the umbilical cord that provides respiration and nourishment for the embryo in addition to eliminating metabolic wastes
    pleiotropy
    most common form of genetic expression in which one gene influences multiple traits
    polygenic trait
    trait influenced by several genes
    preterm (premature/preemie) infant
    any infant born before thirty-seven weeks’ gestation and weighing less than 5.5 lb
    proximodistal growth
    growth that occurs from the center of the body outward
    recessive trait
    trait that requires two identical alleles to be expressed
    single-gene disorder
    condition caused by variation in a single gene
    spontaneous abortion
    (also, miscarriage) loss of a pregnancy during the first twenty weeks
    teratogen
    disease, drug, or environmental agent that can harm an embryo or fetus physically or influence health or behavior after birth
    testes
    parts of the male reproductive system that help create and sustain sperm
    umbilical cord
    a flexible tube connecting the embryo and the placenta
    urethra
    part of the human reproductive system that, in males, transports and releases sperm
    uterus
    part of the female reproductive system where a fertilized egg implants to develop
    vagina
    muscular canal that connects the uterus to the outside of the female body
    vas deferens
    tube that transports sperm from the testes to the urethra
    vulva
    external aspects of the female reproductive system including the labia, clitoris, and vaginal opening
    zygote
    single cell formed at conception and consisting of forty-six chromosomes, twenty-three from each parent

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