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  2. Small supernumerary marker chromosome - Wikipedia

    en.wikipedia.org/wiki/Small_supernumerary_marker...

    Genetic counseling of carriers. A small supernumerary marker chromosome ( sSMC) is an abnormal extra chromosome. It contains copies of parts of one or more normal chromosomes and like normal chromosomes is located in the cell's nucleus, is replicated and distributed into each daughter cell during cell division, and typically has genes which may ...

  3. 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 = { Z1, Z2, ..., Zn }, written ρXY·Z, is the correlation between the residuals eX and eY resulting from the linear regression of X with Z and of Y with Z, respectively. The first-order partial correlation (i.e., when n = 1) is the difference between a ...

  4. Confined placental mosaicism - Wikipedia

    en.wikipedia.org/wiki/Confined_placental_mosaicism

    The pregnancy outcome is strongly chromosome specific. The most frequently seen trisomic cells in confined placental mosaicism involve chromosomes 2, 3, 7, 8 and 16. The next frequently involved are 9, 13, 15, 18, 20 and 22. It has been observed that CPM involving the sex chromosomes usually has no adverse effects on fetal development.

  5. Chromosome 5q deletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Chromosome_5q_deletion...

    Chromosome 5q deletion syndrome is an acquired, hematological disorder characterized by loss of part of the long arm ( q arm, band 5q33.1) of human chromosome 5 in bone marrow myelocyte cells. This chromosome abnormality is most commonly associated with the myelodysplastic syndrome . It should not be confused with "partial trisomy 5q", though ...

  6. Uniparental disomy - Wikipedia

    en.wikipedia.org/wiki/Uniparental_disomy

    Medical genetics. Uniparental disomy ( UPD) occurs when a person receives two copies of a chromosome, or of part of a chromosome, from one parent and no copy from the other. [1] UPD can be the result of heterodisomy, in which a pair of non-identical chromosomes are inherited from one parent (an earlier stage meiosis I error) or isodisomy, in ...

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  8. XYY syndrome - Wikipedia

    en.wikipedia.org/wiki/XYY_syndrome

    Frequency. ~1 in 1,000 males [1] XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. [1] There are usually few symptoms. [2] These may include being taller than average and an increased risk of learning disabilities.

  9. Tetrasomy - Wikipedia

    en.wikipedia.org/wiki/Tetrasomy

    Full. Full tetrasomy of an individual occurs due to non-disjunction when the cells are dividing ( meiosis I or II) to form egg and sperm cells ( gametogenesis ). This can result in extra chromosomes in a sperm or egg cell. After fertilization, the resulting fetus has 48 chromosomes instead of the typical 46.

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