When.com Web Search

Search results

  1. Results From The WOW.Com Content Network
  2. Uniparental disomy - Wikipedia

    en.wikipedia.org/wiki/Uniparental_disomy

    Uniparental inheritance of imprinted genes can also result in phenotypical anomalies. Although few imprinted genes have been identified, uniparental inheritance of an imprinted gene can result in the loss of gene function, which can lead to delayed development, intellectual disability, or other medical problems. [citation needed]

  3. Kagami-Ogata Syndrome - Wikipedia

    en.wikipedia.org/wiki/Kagami-Ogata_Syndrome

    There are three main mechanisms that can cause KOS: [4] Paternal Unipaternal Disomy (in 55-70% cases). This can be caused by monosmy rescue. Usually Paternal UPD arises from nondisjunction in oocyte which causes nullisomy of that chromosome. When such oocyte gets fertilised, conceptus will have 1 chromosome (in that case only one chromosome 14 ...

  4. Isodisomy - Wikipedia

    en.wikipedia.org/wiki/Isodisomy

    Isodisomy is a form of uniparental disomy in which both copies of a chromosome, or parts of it, are inherited from the same parent.It differs from heterodisomy in that instead of a complete pair of homologous chromosomes, the fertilized ovum contains two identical copies of a single parental chromosome.

  5. Angelman syndrome - Wikipedia

    en.wikipedia.org/wiki/Angelman_syndrome

    This can be due to genetic errors such as the deletion or mutation of a segment of chromosome 15, uniparental disomy, or translocation. While Angelman syndrome can be caused by a single mutation in the UBE3A gene, the most common genetic defect leading to Angelman syndrome is a 5- to 7-Mb (megabase) maternal deletion in chromosomal region 15q11 ...

  6. Loss of heterozygosity - Wikipedia

    en.wikipedia.org/wiki/Loss_of_heterozygosity

    Possible causes for copy-neutral LOH include acquired uniparental disomy (UPD) and gene conversion. In UPD, a person receives two copies of a chromosome, or part of a chromosome, from one parent and no copies from the other parent due to errors in meiosis I or meiosis II.

  7. AOL

    search.aol.com

    The search engine that helps you find exactly what you're looking for. Find the most relevant information, video, images, and answers from all across the Web.

  8. Genomic imprinting - Wikipedia

    en.wikipedia.org/wiki/Genomic_imprinting

    Genomic imprinting is an epigenetic phenomenon that causes genes to be expressed or ... if uniparental disomy occurs and a person inherits both chromosomes from the ...

  9. 270 Reasons Women Choose Not To Have Children - The ...

    data.huffingtonpost.com/2015/07/choosing-childfree

    The number of childfree women is at a record high: 48 percent of women between the ages of 18 and 44 don’t have kids, according to 2014 Census numbers. The Huffington Post and YouGov asked 124 women why they choose to be childfree.