Abortion: Premature expulsion of the fetus from uterus.
Aneuploidy: Having an extra or less chromosome related to the parental chromosome number.
Aneuploidy |
Autosome: Chromosome of any type that is the same in males and females of the species.
Crossing Over: Interaction in which non-sister chromatids of homologous chromosome break corresponding sites and exchanges segments.
Deletion: Loss of a segment from a chromosome or loss few base pairs from a DNA molecules.
study
Genetic: Rare or less common version of a heritable trait.
abnormality
disorder
Genetic Disorder |
Genetic:
recombination Results of process that puts new genetic information into a DNA molecules.
Homologous: One of a pair of chromosome identical in size, shape, and that interact at meiosis.
chromosome
Homologous Chromosome |
In-vitro: Conception outside the body.
fertelization
Independent assortment: Mendelian theory that at the end of meiosis, each pair of homologous chromosome are sorted to gametes independently.
Inversion: Part of a chromosome that became oriented in reverse.
Linkage: All genes on a chromosome.
group
Mosaicism: Cells of the same types that express genes differently.
Mosaicism |
Non-disjunction: Failure of a pair of homologous chromosome to separated during meiosis or mitosis.
Polyploidy: Having three or more of each type of chromosome in the nucleus.
Reciprocal cross: Paired cross, in the first 1 parent displays the trai of interest; in the second the other parent displays it.
Sex: Chromosome with genes that affect sexual traits.
chromosome
Syndrome |
Translocation: Movement of a stretch of DNA to a new chromosal location.
X: Type of sex chromosome were the embryo becomes a female.
chromosome
chromosome
Duplication |
Translocation |
Y Chromosome |