Answer: Homologous chromosomes are randomly distributed to daughter cells, this means different chromosomes segregate independently of each other. And they exchange segments of DNA during crossing over. This recombination creates genetic diversity because genes from each parent are exchanged.
Explanation:
Meiosis is a type of cell division that produces gamete cells, which are sex cells (egg and sperm)
Chromosomes that form a pair and are found together are called homologous chromosomes, and they are inherited from each parent. During prophase of meiosis I, the homologous chromosomes exchange segments of DNA in a process called crossing over. This recombination creates genetic diversity because genes from each parent are exchanged. <u>It results in new combinations of genes on each chromosome.</u>
After that, during the anaphase of meiosis I, the two chromosomes line up on the equatorial plane of the cell. Then, they are separated and each will go to a new daughter cell. So homologous chromosomes are randomly distributed to daughter cells, <u>this means different chromosomes segregate independently of each other.</u>
Answer:
Complete question:
We are trying to determine the possible modes of inheritance for some particular human disorder. We have a very small pedigree for this disorder. Assuming the pedigree is accurate, indicate which of the six modes of inheritance are consistent with this pedigree: Select one or more Y Linked Autosomal Recessive Autosomal Dominant X-Linked Dominant X-Linked Recessive We are trying to determine the possible modes of inheritance for some particular human disorder. We have a very small pedigree for this disorder, Assuming the pedigree is accurate, indicate which of the six modes of inheritance ere consistent with this pedigree Select one or more X-Linked Recessive Y Linked Autosomal Recessive X-Linked Dominant Autosomal Dominant.
Answer:
After the analysis of this pedigree, it is clears that the inheritance pattern is X linked because the offsprings are affected with parents genotgype
Explanation:
The inheritance is X linked dominant because of the presence of one dominant gene for the affected genotype in male.
The male individuals are affected. This is therefore not a recessive inheritance in later case, it is only when the two genes are present at the same time the affected genotype will be seen.
oogonia no result of oogonia human
ovogonia:Esto quiere decir que la ovogonia tenía 46 cromosomas como se afirmó anteriormente, y el ovocito debe sufrir una reducción por medio de la denominada Meiosis hasta tener 23 cromosomas, 22 cromosomas somáticos y un cromosoma X (22X), el cual es el número Haploide
I hope it helps you.
Answer:
Space telescopes can carry instruments to observe objects emitting various types of electromagnetic radiation such as visible, infrared or ultraviolet light; gamma rays; or x-rays. X-ray telescopes, such as the Chandra X-ray Observatory, use X-ray optics to observe remote objects in the X-ray spectrum.
Explanation:
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The answer is a<span>ctivation because during this amino acid is activated by aminoacyl-trna synthetase enzyme and added to trna</span>
