Yes, nondisjunction results in a germinal cell (ovum or spermatozoa) with either too many or too few chromosomes. If one of these cells joins with another to form a zygote, there may be one or more too many or too few chromosomes in the cells.
Mutation
Diploid
Genes located on the X or Y chromosome are referred to as sex-linked genes. This is because the inheritance of these genes is dependent upon the sex of the individual. For example, only males can inherit genes located on the Y chromosome (because males have XY and females have XX).
A Haploid
Tell me about Somatic Cells ? Tell me about Somatic Cells ? Tell me about Somatic Cells ?
Having a single copy of each chromosome is called the haploid condition eg in egg and sperm cells.Having pairs of chromosomes is called the diploidcondition eg in all other body cells (except red blood cells which do not have chromosomes).
down syndrome
Down syndrome is a result of having an extra chromosome in one's genes. Chromosome thirteen* if your that much into the science. It is also called trisomy 21 because the chromosome 21 is the one with the abnormalities. *Abnormalities with chromosome thirteen is called Patau syndrome or trisomy 13.
they are chromosomes having secondary contriction.. aka satellite chromosome
they are chromosomes having secondary contriction.. aka satellite chromosome
Diploid
Down syndrome occurs because of the extra chromosome on chromosome 21. If you go onto google images and type in karyotype of Down syndrome, you will find a picture of the extra chromosome. Instead of having two chromosomes on chromosome 21, there is an extra. Type your answer here...
It is the female having one additional X chromosome making her genotype 44 + XXX called meta female It is also called Super female
Down syndrome is a chromosomal disorder. It is caused by having 1 extra chromosome (chromosome 21).
Genes located on the X or Y chromosome are referred to as sex-linked genes. This is because the inheritance of these genes is dependent upon the sex of the individual. For example, only males can inherit genes located on the Y chromosome (because males have XY and females have XX).
Hemophilia occurs in the X chromosome, and males are the genders that have the X chromosome.
Chromatin is intertwinted mass of fine thread-like structure made of DNA and protein. During cell division (mitosis and meiosis), chromatin condenses to form thicker rod-like structures called chromosomes. Each chromosome consists of two similar halves called chromatids. Formation of chromosomes having two similar halves or chromatids is meant for equitable distribution of chromatin which is hereditary material.
It is called prejudice; judging ahead of time; deciding before having any knowledge of an individual what that individual is like, based on pre-determined judgements.