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  2. Monosomy - Wikipedia

    en.wikipedia.org/wiki/Monosomy

    Human conditions due to monosomy: Turner syndrome – Females with Turner syndrome typically have one X chromosome instead of the usual two X chromosomes. Turner syndrome is the only full monosomy that is seen in humans — all other cases of full monosomy are lethal and the individual will not survive development.

  3. Cri du chat syndrome - Wikipedia

    en.wikipedia.org/wiki/Cri_du_chat_syndrome

    Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. [1] Its name is a French term ("cat-cry" or "call of the cat") referring to the characteristic cat-like cry of affected children (sound sample ). [2] It was first described by Jérôme Lejeune in 1963. [3]

  4. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly where a male has an extra X chromosome. [10] These complications commonly include infertility and small, poorly functioning testicles (if present).

  5. ASCII - Wikipedia

    en.wikipedia.org/wiki/ASCII

    ASCII (/ ˈ æ s k iː / ⓘ ASS-kee), [3]: 6 an acronym for American Standard Code for Information Interchange, is a character encoding standard for electronic communication. . ASCII codes represent text in computers, telecommunications equipment, and other devic

  6. Trisomy X - Wikipedia

    en.wikipedia.org/wiki/Trisomy_X

    The prevalence of trisomy X in women with adult-onset schizophrenia is estimated to be around 1 in 400, compared to 1 in 1,000 in women as a whole; the prevalence in childhood onset schizophrenia is unclear, but may be as high as 1 in 40. [25] One in five women with trisomy X report clinically significant levels of anxiety.

  7. Uniparental disomy - Wikipedia

    en.wikipedia.org/wiki/Uniparental_disomy

    For example, either isodisomy or heterodisomy can disrupt parent-specific genomic imprinting, resulting in imprinting disorders. Additionally, isodisomy leads to large blocks of homozygosity , which may lead to the uncovering of recessive genes, a similar phenomenon seen in inbred children of consanguineous partners.

  8. Mouse models of Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Mouse_models_of_Down_syndrome

    The Dp(16)1Yu model (also referred to as Dp(16)1Yey) contains a partial duplication of the mouse chromosome 16 (MMU16). Unlike the Ts65Dn model, Dp(16)1Yu contains a duplication of only the parts of chromosome 16 that are homologous to human chromosome 21. This makes the Dp(16)1Yu model a more genetically accurate representation of Down Syndrome.

  9. Partial correlation - Wikipedia

    en.wikipedia.org/wiki/Partial_correlation

    Formally, the partial correlation between X and Y given a set of n controlling variables Z = {Z 1, Z 2, ..., Z n}, written ρ XY·Z, is the correlation between the residuals e X and e Y resulting from the linear regression of X with Z and of Y with Z, respectively.