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Bio Ch. 8
Chromosomes & Human Genetics
| Term | Definition |
|---|---|
| genetic disorder | a disease caused by a defective gene(s), or an abnormality in chromosome number or structure |
| pedigree | Shows genetic relationships among family members over 2 or more generations of a family’s medical history |
| karyotype | a photograph of a cell’s chromosomes with each set of homologous chromosomes paired up |
| sex chromosome | determine a person’s biological sex |
| autosome | homologous chromosomes exactly alike in length, shape, & genes |
| chromosomal abnormality | any change in the chromosome number or structure, compared to what is typical for a species |
| locus | the physical location of a gene on a chromosome |
| sex-linked | some trait or disease only found on the X or Y chromosome |
| x-linked | some trait or disease only found on the X chromosome |
| y-linked | some trait or disease only found on the Y chromosome |
| genetic carrier | person that carries the disorder allele |
| recessive genetic disorder | include several thousand human genetic disorders that are inherited as recessive traits on autosomes |
| dominant genetic disorder | an inherited disease caused by an autosomal dominant allele |
| gene therapy | a technique for correcting abnormal genes responsible for disease development |
| genetic engineering | the permanent introduction of one or more new or altered genes into a cell, tissue, or organism |
| amniocentesis | a prenatal genetic screening technique in which amniotic fluid is extracted from the pregnancy sac that surrounds a fetus by means of a needle that is inserted through the abdomen into the uterus |
| chorionic villus sampling (CVS) | a prenatal genetic screening technique in which cells are extracted by gentle suction from the villi (a cluster of cells that attaches the pregnancy sac to the wall of the uterus) |
| in vitro fertilization (IVF) | fertilization of an egg by a sperm in a petri dish, followed by implantation of one or more embryos into a woman's uterus |
| preimplantation genetic diagnosis (PGD) | the removal of one or two cells from an embryo developing in a petri dish, usually 3 days after fertilization, followed by testing for genetic disorders |
| stem cells | unique, unspecialized cells that can make identical copies of themselves for long periods of time |
| mutation | changes to DNA sequences, or chromosome number or structure |