When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_18

    G-banding patterns of human chromosome 18 in three different resolutions (400, [12] 550 [13] and 850 [3]). Band length in this diagram is based on the ideograms from ISCN (2013). [ 14 ] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process .

  3. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    Karyotype of a person with trisomy 18. Three copies of the Chromosome 18 are detected. Trisomy 18 is a chromosomal abnormality characterized by the presence of an extra copy of genetic material on the 18th chromosome, either in whole (trisomy 18) or in part (such as due to translocations). The additional chromosome usually occurs before ...

  4. Chromosome 18 (human) - Wikipedia

    en.wikipedia.org/?title=Chromosome_18_(human...

    Pages for logged out editors learn more. Contributions; Talk; Chromosome 18 (human)

  5. Category:Chromosomes (human) - Wikipedia

    en.wikipedia.org/wiki/Category:Chromosomes_(human)

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  6. Category:Genes on human chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Category:Genes_on_human...

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  7. Tetrasomy 18p - Wikipedia

    en.wikipedia.org/wiki/Tetrasomy_18p

    Tetrasomy 18p is caused by the presence of an additional isochromosome composed of two copies of the p arm of chromosome 18. [4] This extra chromosome is classified as a small supernumerary marker chromosome that forms de novo in a parent's egg or sperm or, in rare cases, is directly inherited from a parent carrier of the intact small ...

  8. C18orf63 - Wikipedia

    en.wikipedia.org/wiki/C18orf63

    This gene is located at band 22, sub-band 3, on the long arm of chromosome 18. It is composed of 5065 base pairs spanning from 74,315,875 to 74,359,187 bp on chromosome 18. [5] The gene has a total of 14 exons. [5] C18orf63 is also known by the alias DKFZP78G0119. [8] No isoforms exist for this gene. [5] NCBI GEO Expression Profile for C18orf63

  9. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Proximal 18q-is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18.This deletion involves the proximal (near the centromere) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [1]