Watson And Crick Turner Syndrome

Also, scientists are now able to identify specific chromosomes involved in certain disorders such as Down Syndrome, Turner Syndrome, and Klinefelter Syndrome. An individual with Down Syndrome has an extra copy of chromosome 21 (“Chromosomal Abnormalities,” par. 1). Only women can have Turner Syndrome which occurs when a female has only one X chromosome. Females with this disorder may have an array of developmental and medical problems; they are also sterile (“Turner Syndrome,” par. 1). Klinefelter Syndrome, which occurs when a male has an extra X chromosome, affects cognitive and physical development (“Klinefelter Syndrome,” par. 1). In addition to these disorders, there are also sex-linked disorders like colorblindness, hemophilia, and muscular dystrophy. One must also consider recessive disorders, dominant disorders, and codominant disorders which have been identified and understood partly because of Watson and Crick’s DNA research.
Anyone involved in the study of DNA borrows from the learning of Crick and Watson, along with many other scientists. Clearly, Crick and Watson made a great team; they impacted the history of science and paved the road for future discoveries. People now have a much better understanding of DNA, genes, genetic disorders, and health thanks to Crick. Things like DNA tests, cloning, new medicines, and genetic engineering have developed due to past discoveries of the nature and structure of DNA. Modern scientists, who focus on DNA, can thank Crick for his contributions to the