In genetics, a chromosome is a threadlike structure of nucleic acids and protein which is located in the nucleus of living cells, It carries the genetic information of an organism in the form of genes.
a chromosome is made up of DNA, which is made up of genes, your chromosomes do decide how your life goes, they decide everything from gender to eye colour and are in every one of your cells, humans have 46 chromosome's, 23 pairs, chromosomes always come in pairs. Other animals have many different numbers of pairs.
the genotypes of their parents
Technically we have 23 chromasomes (you will never hear a paper refer to chromasome 24 or 37 etc), but we have two copies of each, bringing the total to 46. This includes the sex chromasomes.
Gametes are haploid cells which means they have only half the normal number of somatic cell (diploid). Somatic cells have 46 chromasomes, organised into 23 pairs, and gametes have only one chromasome from each pair.
an allele that is not expressed when paired with a dominant allele. Only expressed when paired with another recessive allele.
1. primary spermatocyte (dipolotid (46)) ------1st meiotic division------ produce: 2 secondary spermatocytes (haploid (23)) ------2nd meiotic division-------- Producing four spermatids (haploid (23)) so the difference is that in the begnning u have a dipoloid cell with 46 chromosomes, and in the end u wil have a haploid cell with 23 chromosomes that in the case are ready to meet the egg, and produce a zygote (diplotid, with 46 chromosomes) that wil develop to be a child.
the genotypes of their parents
Yes- it is transmitted from parent to child by a chromasome.
soul life Carabanna chromatic Chromasome
it's the duplication of the 21st chromasome
Females are rarely colourblind because they have 2 X chromasomes. They would therefore have to have inherited the gene from both parents (X from the mother and X from the father). As males have only 1 X chromasome and there is no corresponding place on the Y chromasome for the matching allele (gene), men who inherit the gene on the X chromasome (from their mothers) are automatically colourblind.
Yes- but only in the case of a genetic disease that is carried ONLY on the Y chromasome.
Technically we have 23 chromasomes (you will never hear a paper refer to chromasome 24 or 37 etc), but we have two copies of each, bringing the total to 46. This includes the sex chromasomes.
The sperm cell is haploid (has half as many chromasomes as the diploid nerve cell)The sperm cell can contain more mutations (depending on the age of the man, this is the basis of anticipation)The sperm cell's chromasome has undergone recombination (I'm assuming you know what that is)
well 8i think this could be a hereditary condition called gingerism in which the chromasome for pube legnth is crossed over with the smell gene on the 18th chromasomje creating this effect sollution== wash, deoderize or shave ur smelly areas if this problem continues after you have done all three you have cancer of the pubism
Gametes are haploid cells which means they have only half the normal number of somatic cell (diploid). Somatic cells have 46 chromasomes, organised into 23 pairs, and gametes have only one chromasome from each pair.
Color blindness is a sex-linked genetic disorder. The reason that it is more prevalent in males is because the disorder is linked the the X-chromasome. If a male inherits an X chromosome that is defective, then they will be color blind. However, a female has two X chromosomes which means she can receive a defective chromosome and only be a carrier of the mutation. If she receives two defective x chromosomes, she will be colorblind.
An individual with Down Syndrome has the presence of all or part of an extra 21st chromosome.