nuclear matrix
An extra chromosome can cause genetic disorders such as Down syndrome, which is caused by an extra copy of chromosome 21. This leads to developmental delays, intellectual disabilities, and certain physical characteristics.
To what structure in female is the vas deferend similar in function.
Probably the Great Pyramid.
Muscle type is polygenic and is probably influenced early on during the gastrulation phase. Since there is substantial variation within families all the alleles are not on the same chromosome.
Based on your history, you are probably talking about colorblindness, which is a disease inherited on the X chromosome. When it is passed on to a boy, the recessive allele shows itself because boys only have one X chromosome. Edited answer: Though recessive alleles do not express but if it adds to a deficiecy it is reflected in the boy, because only one X chromosome in present there, the other being Y chomosome which is almost enert.
If a piece of DNA breaks off a chromosome and attaches itself to a nonhomologous chromosome at another location translocation is the type of change that has occurred. The chromosomal pieces are moved to a new location.
Chromosome 16 has been a target of study by Crohns disease researchers lately and Chromosome 16 probably contains between 850 and 1,200 genes.
Probably a face-centered cubic structure.
Probably
The X chromosome. That's why it's more common in males; females have 2 X chromosomes, but males only have 1. So if a woman has the hemophilia mutation on one of her chromosomes, she probably won't be affected by it.
chewing
Structure is probably the word you are looking for.
The Location would probably be at a Park. In a nice quiet area.
A map, probably.
To what structure in female is the vas deferend similar in function.
An extra chromosome can cause genetic disorders such as Down syndrome, which is caused by an extra copy of chromosome 21. This leads to developmental delays, intellectual disabilities, and certain physical characteristics.
chewing