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A comprehensive set of vocabulary flashcards covering genetics, fertilization, early embryology, gestation, placental development, germ layers, and postnatal development.
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Genes
Sequence of DNA that provides instructions for making a polypeptide (or RNA) product.
Genotype
The genetic constitution of an organism—the set of genes and alleles it carries.
Phenotype
The observable expression of a genotype, i.e., the physical/biochemical traits produced.
Homologous chromosomes
Pairs of chromosomes that are similar in size and gene content, one from each parent.
Autosomes
Chromosomes 1-22 that are not sex chromosomes.
Sex chromosomes
Chromosomes X and Y; determine sex and often carry sex-linked genes.
X chromosome
A sex chromosome; carries many genes; in males it is the single X with no corresponding Y allele.
Y chromosome
A sex chromosome; carries genes that determine maleness and X-linked gene interactions.
Locus
The specific location of a gene on a chromosome.
Alleles
Different versions of a gene that can occupy the same locus.
Homozygous
Having two identical alleles for a gene.
Heterozygous
Having two different alleles for a gene.
Simple (monohybrid) inheritance
Inheritance determined by a single gene pair; phenotype influenced by one allele pair.
Polygenic inheritance
Phenotype determined by interactions among alleles of multiple genes.
Sex-linked inheritance
Inheritance involving genes on the sex chromosomes, often X-linked.
X-linked
Genes located on the X chromosome; often expressed differently in males and females.
Dominant
An allele that masks the expression of other alleles for a trait.
Recessive
An allele whose trait is masked by a dominant allele when present with it.
Codominance
Both alleles are expressed in the phenotype (e.g., AB blood type).
Incomplete dominance
Two alleles produce an intermediate phenotype rather than a dominant/recessive pattern.
Zygote
The diploid cell formed by the fusion of sperm and egg.
Cleavage
Mitosis of the zygote without growth in cytoplasmic volume.
Morula
A solid ball of cells (3-4 days after fertilization) formed during early development.
Blastocyst
A hollow sphere of cells with an inner cell mass and trophoblast; implants into the endometrium.
Trophoblast
Outer cell layer of the blastocyst that contributes to the placenta.
Embryoblast
Inner cell mass of the blastocyst; develops into the embryo.
Implantation
Attachment of the blastocyst to the endometrium, enabling pregnancy to proceed.
Placenta
An organ formed by embryonic (chorionic villi) and maternal tissues that exchanges nutrients, wastes, gases, and hormones between mother and fetus.
Chorionic villi
Finger-like projections from the chorion that invade the endometrium and allow fetal blood vessels to develop.
Amnion
The extraembryonic membrane that forms the amniotic cavity and protects the developing embryo.
Yolk sac
An early extraembryonic membrane source of nutrients and blood cell formation.
Allantois
An extraembryonic membrane that contributes to the umbilical cord and bladder formation.
Umbilical cord
Cord containing fetal vessels that connects the fetus to the placenta.
Preembryonic period
0–16 days after fertilization; includes zygote, cleavage, morula, blastocyst, and implantation.
Embryonic period
Weeks 3–8; organ and germ layer formation (differentiation and development of tissues).
Fetal period
Weeks 9–birth; growth and maturation of organs and systems.
Gastrulation
Formation of the three primary germ layers: ectoderm, mesoderm, endoderm.
Germ layers
Ectoderm (outer), mesoderm (middle), endoderm (inner) that give rise to all tissues.
Ectoderm
Germ layer that forms skin, nervous system, and related structures.
Mesoderm
Germ layer that forms bones, muscles, cardiovascular system, and more.
Endoderm
Germ layer that forms the lining of the digestive and respiratory tracts and associated glands.
Embryonic disc
Early embryonic structure; will differentiate into the body plan and germ layers.
Differentiation
Process by which cells become specialized in structure and function.
Induction
Signaling interactions that cause one group of cells to become something different.
Chorion
Fetal membrane that forms part of the placenta and surrounds the amniotic sac.
Amniotic cavity
Fluid-filled cavity within the amnion surrounding the developing embryo.
Placental exchange
Nutrients diffuse from maternal blood to fetal blood; wastes diffuse in the opposite direction.
Epigenetics
Heritable changes in gene expression not due to DNA sequence changes.
Imprinting
A type of epigenetic modification where gene expression depends on parental origin.
Nondisjunction
Failure of chromosome pairs to separate properly during meiosis, leading to abnormal chromosome numbers.
Disjunction
Normal separation of homologous chromosomes or sister chromatids during meiosis.
Turner syndrome
XO phenotype; female with a missing or structurally abnormal second sex chromosome.
Triple X syndrome (XXX)
Females with an extra X chromosome; often taller and may have developmental differences.
Dizygotic twinning
Fraternal twins from two separate fertilizations (two zygotes).
Monozygotic twinning
Identical twins from a single fertilized egg that splits.
Ovulation
Release of a secondary oocyte from the ovary prior to fertilization.
Capacitation
Maturation of sperm that enables fertilization, including increased motility and receptor exposure.
Acrosome reaction
Release of enzymes from the sperm acrosome that help penetrate the zona pellucida.
Corona radiata
Outer protective layer of cells surrounding the oocyte.
Zona pellucida
Glycoprotein layer surrounding the oocyte that sperm must penetrate during fertilization.
Fertilization
Fusion of sperm and oocyte nuclei forming a zygote.
Pronuclei
Male and female nuclei inside the zygote before they fuse to form the diploid genome.
Polyspermy prevention
Blockades (e.g., cortical reaction) that prevent more than one sperm from fertilizing the egg.
Epithelium
A type of tissue formed from germ layers; lines organs and structures.