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Mirroring chromosomes are a genetic abnormality. This abnormality is caused by an exact duplication of a chromosome segment, including the centromere.
can be inherited as the result of a dominant genetic abnormality (only one parent carries the abnormal gene) or a recessive genetic abnormality (both parents carry the abnormal gene).
It's genetic, and recessive - get a test to see if you're a carrier. If you already have it than wait until gene manipulation becomes common.
Is the genetic abnormality which is a characteristic of a haematological malignancy, chronic myeloid leukemia.
The Philadelphia chromosome abnormality is that chromosome 9 and 22 have swapped places. This abnormality causes a higher susceptibility to forms of leukemia. Specificly it is connected most commonly to chronic myelogenous leukemia.
HIV is the virus that causes HIV. It is not a genetic abnormality.
Phenylketonuria
The best treatment of phenylketonuria is a diet that is extremely low in phenylalanine during childhood. A person can also take fish oil supplements and iron supplements to help treat some of the symptoms.
Phenylketonuria (PKU) is a rare genetic condition that is present from birth. It is a learning disability that can damage the brain.
Phenylketonuria is a genetic disorder that was first discovered in 1934 by Dr. Asbjorn Folling of Norway
Phenylketonuria (PKU) is the human genetic defect that results in the failure to metabolize the amino acid phenylalanine.
Phenylketonuria
Phenylketoneuria is the name of a rare genetic disorder, not a chemical compound.
mutation
A genetic syndrome simply defined is: a disease caused by an abnormality in an individual's genetic make-up.
phenylketonuria
Mirroring chromosomes are a genetic abnormality. This abnormality is caused by an exact duplication of a chromosome segment, including the centromere.