enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Distal trisomy 10q - Wikipedia

    en.wikipedia.org/wiki/Distal_trisomy_10q

    Distal trisomy 10 is a rare chromosomal disorder that causes several physical defects and intellectual disability. [5] Humans, like all sexually reproducing species, have somatic cells that are in diploid [2N] state, meaning that N represent the number of chromosomes, and 2 the number of their copies. In humans, there are 23 chromosomes, but ...

  3. Aneuploidy - Wikipedia

    en.wikipedia.org/wiki/Aneuploidy

    Aneuploidy is the presence of an abnormal number of chromosomes in a cell, for example a human cell having 45 or 47 chromosomes instead of the usual 46. [1][2] It does not include a difference of one or more complete sets of chromosomes. A cell with any number of complete chromosome sets is called a euploid cell. [1]

  4. Trisomy - Wikipedia

    en.wikipedia.org/wiki/Trisomy

    The number of chromosomes in the cell where trisomy occurs is represented as, for example, 2n+1 if one chromosome shows trisomy, 2n+1+1 if two show trisomy, etc. [2] "Full trisomy", also called "primary trisomy", [2] means that an entire extra chromosome has been copied. "Partial trisomy" means that there is an extra copy of part of a chromosome.

  5. Pallister–Killian syndrome - Wikipedia

    en.wikipedia.org/wiki/Pallister–Killian_syndrome

    The Pallister–Killian syndrome (PKS), also termed tetrasomy 12p mosaicism or the Pallister mosaic aneuploidy syndrome, is an extremely rare and severe genetic disorder. PKS is due to the presence of an extra and abnormal chromosome termed a small supernumerary marker chromosome (sSMC). sSMCs contain copies of genetic material from parts of ...

  6. Trisomy X - Wikipedia

    en.wikipedia.org/wiki/Trisomy_X

    approximately 1 in 1,000 (female) Trisomy X, also known as triple X syndrome and characterized by the karyotype [note 1] 47,XXX, is a chromosome disorder in which a female has an extra copy of the X chromosome. It is relatively common and occurs in 1 in 1,000 females, but is rarely diagnosed; fewer than 10% of those with the condition know they ...

  7. Ring chromosome - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome

    A ring chromosome is an aberrant chromosome whose ends have fused together to form a ring. Ring chromosomes were first discovered by Lilian Vaughan Morgan in 1926. [1] A ring chromosome is denoted by the symbol r in human genetics and R in Drosophila genetics. Ring chromosomes may form in cells following genetic damage by mutagens like ...

  8. TODAY/AOL 'Ideal to Real' body image survey results

    www.aol.com/lifestyle/2014-02-24-loveyourselfie...

    TODAY/AOL 'Ideal to Real' body image survey results. Brynn Mannino. Updated July 14, 2016 at 10:10 PM. Show comments. Feedback. Help. Join AOL. Accessibility. EU Digital Services Act.

  9. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    The extra chromosome content can arise through several different ways. The most common cause (about 92–95% of cases) is a complete extra copy of chromosome 21, resulting in trisomy 21. [91] [96] In 1–2.5% of cases, some of the cells in the body are normal and others have trisomy 21, known as mosaic Down syndrome.