Use of chromosome in Sentences. 47 Examples

The examples include chromosome at the start of sentence, chromosome at the end of sentence and chromosome in the middle of sentence

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chromosome at the end of sentence


  1. It is carried on the X chromosome.
  2. It is carried on the X chromosome.
  3. The scientists want to locate the position of the gene on a chromosome.
  4. The scientists want to locate the position of the gene on a chromosome.
  5. In man, for instance, the genes that control gender are on the Y chromosome.
  6. In man, for instance, the genes that control gender are on the Y chromosome.
  7. However, the genes brought in by a plasmid do not usually become a permanent part of the bacterium's own chromosome.
  8. However, the genes brought in by a plasmid do not usually become a permanent part of the bacterium's own chromosome.

chromosome in the middle of sentence


  1. The cytoplasmic apparatus thus effects chromosome division.
  2. Research that will identify a funny gene or chromosome or whatever.
  3. The grey regions indicate either chromosome breaks or missing data.
  4. Research that will identify a funny gene or chromosome or whatever.
  5. A visible example of X chromosome inactivation is the tortoiseshell cat.
  6. A visible example of X chromosome inactivation is the tortoiseshell cat.
  7. Lane 1 corresponds to a cosmid from human chromosome 6 and serves as a control.
  8. Lane 1 corresponds to a cosmid from human chromosome 6 and serves as a control.
  9. The nuclear membrane will not be re-formed until chromosome division is complete.
  10. The nuclear membrane will not be re-formed until chromosome division is complete.
  11. Around Roscoff, Staiger found shell thicknesS to be associated with chromosome number.
  12. Around Roscoff, Staiger found shell thicknesS to be associated with chromosome number.
  13. The gene is found on the X chromosome, males being more severely affected than females.
  14. Every cell contains two chromosome 9s, and two versions of location 7230 along chromosome 9.
  15. Every cell contains two chromosome 9s, and two versions of location 7230 along chromosome 9.
  16. Consequently, a Cain gene on an X chromosome can safety kill the Y chromosome and not risk suicide.
  17. When they form bivalents, however, each chromosome is in close physical contact with its homologue.
  18. When they form bivalents, however, each chromosome is in close physical contact with its homologue.
  19. Plasmid: circular DNA molecules able to replicate independently of the chromosome in microorganisms.
  20. Plasmid: circular DNA molecules able to replicate independently of the chromosome in microorganisms.
  21. The fetus becomes male only when it both has a Y chromosome and is acted upon by androgenic hormones.
  22. Oct-11a is located in a region of mouse chromosome 9 homologous with the long arm of human chromosome 11.
  23. They also always deliver their package of genes into the host chromosome, integrating more or less at random.
  24. This suggests that the human homologue of the Oct-11a locus will reside on chromosome 11 in the region of q23.
  25. This suggests that the human homologue of the Oct-11a locus will reside on chromosome 11 in the region of q23.
  26. At this point esch chromosome consist of a pair of chromatids and the two associated chromosomes are termed a tetrad.
  27. At this point esch chromosome consist of a pair of chromatids and the two associated chromosomes are termed a tetrad.
  28. Two large studies have shown genetic lesions, including chromosome 17p, 18q, and 1p deletion, to be prognostic indicators.
  29. The handicap is caused by a chromosomal abnormality which basically means that there is an additional chromosome in the cells.
  30. Partial chromosome 9 and chromosome 1 linkage maps showing the location of Oct-11a and Oct-11b in relation to linked genes are shown.
  31. Partial chromosome 9 and chromosome 1 linkage maps showing the location of Oct-11a and Oct-11b in relation to linked genes are shown.
  32. Deletions of chromosome 17p are found in 75% of colorectal cancers and are highly correlated with mutation of the remaining p53 gene.
  33. Deletions of chromosome 17p are found in 75% of colorectal cancers and are highly correlated with mutation of the remaining p53 gene.
  34. By estimating the expected number of each chromosome and comparing it with the observed number, any significant departures can be recorded.
  35. In heterozygous females, pre-B cells whose active X chromosome expresses the mutant gene would not terminally differentiate and proliferate.
  36. And each chromosome carries some fifty thousand genes, which are the structures that carry inheritance information from parent to offspring.
  37. And each chromosome carries some fifty thousand genes, which are the structures that carry inheritance information from parent to offspring.
  38. However, over-exposure to the arrestant is detrimental in that male and female complements lose their morphological identity due to chromosome contraction.
  39. However, over-exposure to the arrestant is detrimental in that male and female complements lose their morphological identity due to chromosome contraction.

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stockily -
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