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. 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.

  3. DiGeorge syndrome - Wikipedia

    en.wikipedia.org/wiki/DiGeorge_syndrome

    DiGeorge syndrome is caused by a heterozygous deletion of part of the long arm (q) of chromosome 22, region 1, band 1, sub-band 2 (22q11.2). Approximately 80-90% of patients have a deletion of 3 Mb and 8% have a deletion of 1.5Mb.

  4. 10q26 deletion - Wikipedia

    en.wikipedia.org/wiki/10q26_deletion

    10q26 deletion is an extremely rare genetic syndrome caused by terminal deletion of the long arm of chromosome 10 at 10q26. It is usually a de novo mutation.

  5. 16p11.2 duplication syndrome - Wikipedia

    en.wikipedia.org/wiki/16p11.2_duplication_syndrome

    16p11.2 duplication syndrome is a genetic condition caused by duplication of region on chromosome 16. The odds of developing autism spectrum disorder are elevated and comparable to the rate with 16p11.2 deletion. The rate of having ADHD is higher than in people with deletion.

  6. 1q21.1 duplication syndrome - Wikipedia

    en.wikipedia.org/wiki/1q21.1_duplication_syndrome

    The structure of 1q21.1 is complex. The area has a size of approximately 6 Megabase (Mb) (from 141.5 Mb to 147.9 Mb). Within 1q21.1 there are two areas where a duplication or deletion can be found: the TAR-area for the TAR syndrome and the distal area for other anomalies.

  7. Chromosome 15q trisomy - Wikipedia

    en.wikipedia.org/wiki/Chromosome_15q_trisomy

    duplication 15 q. Chromosome 15q duplication is an extremely rare genetic disorder in which there is an excess copy of a segment of DNA found on the long ("q") arm of human chromosome 15. As a result, affected cells contain a total of 3 copies of the duplicated bases, instead of the usual 2 copies - one inherited from the mother and one from ...

  8. Chromosome 10 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_10

    Chromosome 10 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 10 spans about 134 million base pairs (the building material of DNA ) and represents between 4 and 4.5 percent of the total DNA in cells .

  9. Gene duplication - Wikipedia

    en.wikipedia.org/wiki/Gene_duplication

    Gene duplication (or chromosomal duplication or gene amplification) is a major mechanism through which new genetic material is generated during molecular evolution. It can be defined as any duplication of a region of DNA that contains a gene .

  10. Big Ten Conference - Wikipedia

    en.wikipedia.org/wiki/Big_Ten_Conference

    Big Ten schools also play in two of the 10 largest on-campus basketball arenas in the country: Ohio State's Value City Arena and Maryland's Xfinity Center. Additionally, arenas at Indiana, Wisconsin, Illinois, Iowa, and Penn State rank among the 20 largest on-campus basketball facilities in the United States.

  11. 1q21.1 copy number variations - Wikipedia

    en.wikipedia.org/wiki/1q21.1_copy_number_variations

    1q21.1 copy number variations (CNVs) [1] are rare aberrations of human chromosome 1 . In a common situation a human cell has one pair of identical chromosomes on chromosome 1. With the 1q21.1 CNVs one chromosome of the pair is not complete because a part of the sequence of the chromosome is missing, or overcomplete, because some parts of the ...