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  2. Down syndrome - Wikipedia

    en.wikipedia.org/wiki/Down_syndrome

    Down syndrome (United States) or Down's syndrome (United Kingdom and other English-speaking nations), also known as trisomy 21, is a genetic disorder caused by the presence of all or part of a third copy of chromosome 21. [3]

  3. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    However, this study included young patients, many of whom were too young to exhibit signs of certain psychiatric conditions. The typical age of onset for many of these conditions appears to be during the teen years. Thus, the results of this study may actually underestimate the true incidence of psychiatric conditions within this population.

  4. Isochromosome - Wikipedia

    en.wikipedia.org/wiki/Isochromosome

    Isochromosome in which the arms are mirror copies of each other. An isochromosome is an unbalanced structural abnormality in which the arms of the chromosome are mirror images of each other. [1]

  5. Williams syndrome - Wikipedia

    en.wikipedia.org/wiki/Williams_syndrome

    Williams syndrome (WS), also Williams–Beuren syndrome (WBS), is a genetic disorder that affects many parts of the body. [2] Facial features frequently include a broad forehead, underdeveloped chin, short nose, and full cheeks. [2]

  6. Partial derivative - Wikipedia

    en.wikipedia.org/wiki/Partial_derivative

    It can be thought of as the rate of change of the function in the -direction.. Sometimes, for = (,, …), the partial derivative of with respect to is denoted as . Since a partial derivative generally has the same arguments as the original function, its functional dependence is sometimes explicitly signified by the notation, such as in:

  7. Tetrasomy - Wikipedia

    en.wikipedia.org/wiki/Tetrasomy

    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.

  8. Smith–Magenis syndrome - Wikipedia

    en.wikipedia.org/wiki/Smith–Magenis_syndrome

    Smith–Magenis syndrome (SMS), also known as 17p- syndrome, is a microdeletion syndrome characterized by an abnormality in the short (p) arm of chromosome 17. [1] It has features including intellectual disability, facial abnormalities, difficulty sleeping, and numerous behavioral problems such as self-harm.

  9. Form 10-Q - Wikipedia

    en.wikipedia.org/wiki/Form_10-Q

    Form 10-Q, (also known as a 10-Q or 10Q) is a quarterly report mandated by the United States federal Securities and Exchange Commission, to be filed by publicly traded corporations. Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934, the 10-Q is an SEC filing that must be filed quarterly with the US Securities and Exchange ...