Triple X syndrome is a form of chromosomal variation characterized by the presence of an extra X chromosome in each cell of a human female. The condition occurs only in females, which have an additional chromosome, resulting in the formation of XXX.
The female may not experience severe phenotypic characteristics though because of Barr Bodies. 2 (randomly selected) of the 3 X chromosomes will be "switched off" in each cell.
The human cell is most likely from a female individual. Barr bodies are inactivated X chromosomes in females, and the absence of a Y chromosome indicates that the individual does not have male sex chromosomes.
Homologous chromosomes are pairs of chromosomes (one from the female and one from the male), each of which contains genes which correspond to the genes on the other chromosome in the pair. For example, if a chromosome contains a gene for eye color, the corresponding chromosome will also have a gene for eye color in the same place.
The word that describes similar chromosomes, one from each parent is homologous. Each human for example has, with certain exceptions 23 chromosome pairs. Twenty two are called autosomal meaning having basically to do with the body. These pairs are homologous. The remaining are the sex chromosomes, X and Y. Homologous chromosomes have the potential to contain exactly the same genes, but nature has made sure that they don't.
the female egg cell is almost like a body cell the sperm cell however has 3 sections. A tail for moving, a mid section full of energy producing mitochondria, and a head containing the nucleus and covered with enzymes.
Homologous chromosome have gene of same character.
A female grasshopper typically has 24 chromosomes.
The molecular cause of Pick disease are a series of mutations linked to chromosomes 17, 9 and 3
Normal females have XX chromosomes (unless there is some chromosomal abnormalities such as Turner's Syndrome or fragile X syndrome). It is also possible for a female to have 3 or even X, in which case, she is referred to as a "superfemale"
More information is needed to answer. Please note the disease about which you're asking. Many diseases have a "type 3."
Symptoms of Type 3 Gaucher disease begin during early childhood with symptoms like Type 1.
the combination of sex chromosomes for a female is XXX it is the triple x because in 1947 a women in North Bonerville Africa found that women have 3 sex chromosomes while males only have two
Unlike Type 2, the progress of Type 3 Gaucher disease is slower, although it also includes nervous system damage.
page 314 Huntington's disease is lethal GENETIC DISORDER caused by a rare dominant allele. It's not a chromosonal disease, it is a genetic disorder. D
the combination of sex chromosomes for a female is XXX it is the triple x because in 1947 a women in North Bonerville Africa found that women have 3 sex chromosomes while males only have two
Female ants have only 2 chromosomes, males are haploid, they have only one. This is the smallest number of chromosomes for any animal.
The human cell is most likely from a female individual. Barr bodies are inactivated X chromosomes in females, and the absence of a Y chromosome indicates that the individual does not have male sex chromosomes.
VWD is classified into three basic types: type 1, type 2, and type 3.