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1) the genes and chromosomes do not double after each generations because parental sex cells are haploid and only contain one set of chromosomes. During fertilization the two cells fuse to form a diploid zygote with two copies of genes and chromosomes. For example a normal human has 46 chromosomes (2 copies of 23 chromosomes) during reproduction gametes which contain 23 chromosomes (haploid) fuse to form an offspring with the correct number of chromosomes ( 23 + 23 = 46).
2) offspring only receive one set of chromosomes from each parent so to maintain the chromosome number of humans. If this did not happen you would not be the same species.
Answer:
Replacing skin defects has witnessed several developments over the centuries. It started with the introduction of skin grafting by Reverdin in 1871. Since then, varieties of skin grafting techniques have been used successfully. Despite being clinically useful, skin grafts have many limitations including the availability of the donor site especially in circumstances of extensive skin loss, immune rejection in allogenic skin grafts, pain, scarring, slow healing and infection.1,2 For these reasons, scientist have worked hard to find skin substitutes to replace skin defects without the need for a "natural" skin graft. These materials which are used to cover skin defects are called "Skin substitutes". This article briefly discusses the common types of skin substitutes and their clinical uses.
Reproduction. I hope this helps!