Genetic anomalies where the normal compliment of chromosomes is either more or less than the expected value. In humans the most common trisomy occurs with chromosome 21 and results in Down Syndrome. Very few instances of fewer than a 2N chromosome count result in viable offspring although a child with a single X (sex chromosome) can reach term.
If retardation is caused by chromosomal or other genetic disorders, it is often apparent from infancy.
Chromosomal disorders are caused by abnormalities in the chromosomes.
Chromosomal disorders are caused by abnormalities in the chromosomes.
The genetic code is carried by the molecule in most organisms. chromosomal DNA guanine hereditary?
Jack H. Jung has written: 'Genetic syndromes in communication disorders' -- subject(s): Genetic disorders, Genetics, Genetic aspects, Communicative disorders, Inborn Genetic Diseases, Communication Disorders
Deletion
Two genetic disorders are Turner's syndrome and cystic fibrosis.
Chromosomal Dna.
Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
Chromosomal defects in offspring. Because no genetic material is lost with inversion of genetic material, individuals often have no obvious physical effects. The major risk with the inversion of genetic material is that offspring of these individuals may have more severe chromosomal abnormalities.
Genetic Disorders are caused By a change in a person's DNA. Recessive alleles is the most human genetic disorder.
There are many but in cases there are none.