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Bio Ch. 8

Chromosomes & Human Genetics

TermDefinition
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
Created by: nat.riv
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