Answer:
the ethics of using information from genomes at the individual level
Explanation:
The human genome project (PGH) aims to identify all genes responsible for our normal and pathological characteristics. Long-term results will surely revolutionize medicine, especially in the area of prevention. Thousands of genes can be analyzed at the same time, and people will be able to know if they have an increased predisposition to certain diseases, such as diabetes, cancer, hypertension, or Alzheimer's disease, and treat themselves before symptoms appear.
Alongside these advances, numerous ethical issues are already being discussed and others will arise. These ethical issues are a major challenge to human genome sequencing, and among these issues, the ethics of using genome information at the individual level have been the most challenging.
100% of offspring will be affected. The father is affected and is homozygous dominant, the mother is unaffected and is homozygous recessive. Since there are homzygous dominant genes present, they will always be there to cover the recessive genes, therefore, all offspring will be affected. Hope this helps! (:
C.Stimulation of thoracic or lumbar spinal regions,chain ganglion,acetylcholine release
How are new alleles created? Occasionally, DNA mutations occur in germ cells – cells destined to become eggs or sperm. In this case, the DNA mutation is copied into every new cell of the growing embryo following fertilisation. ... If the mutation affects a gene, it will result in a new version of that gene – a new allele.
