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  2. Chromosome 9 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_9

    Chromosome 9 is one of the 23 pairs of chromosomes in humans.Humans normally have two copies of this chromosome, as they normally do with all chromosomes. Chromosome 9 spans about 138 million base pairs of nucleic acids (the building blocks of DNA) and represents between 4.0 and 4.5% of the total DNA in cells.

  3. Monosomy 9p - Wikipedia

    en.wikipedia.org/wiki/Monosomy_9p

    Monosomy 9p (also known as Alfi's Syndrome, 9p Minus or simply 9P-) is a rare chromosomal disorder in which some DNA is missing or has been deleted on the short arm region, "p", of one copy of chromosome 9 (9p22.2-p23). [1] [2] This deletion either happens de novo or as a result of a parent having the chromosome abnormality. [3]

  4. Oncogene - Wikipedia

    en.wikipedia.org/wiki/Oncogene

    This chromosome was discovered in 1960 by Peter Nowell and David Hungerford, and it is a fusion of parts of DNA from chromosome 22 and chromosome 9. The broken end of chromosome 22 contains the "BCR" gene, which fuses with a fragment of chromosome 9 that contains the "ABL1" gene. When these two chromosome fragments fuse the genes also fuse ...

  5. Low copy repeats - Wikipedia

    en.wikipedia.org/wiki/Low_copy_repeats

    In humans, chromosomes Y and 22 have the greatest proportion of SDs: 50.4% and 11.9% respectively. [2] SRGAP2 is an SD. Misalignment of LCRs during non-allelic homologous recombination (NAHR) [ 3 ] is an important mechanism underlying the chromosomal microdeletion disorders as well as their reciprocal duplication partners. [ 4 ]

  6. Cytogenetics - Wikipedia

    en.wikipedia.org/wiki/Cytogenetics

    This abnormal chromosome was dubbed the Philadelphia chromosome - as both scientists were doing their research in Philadelphia, Pennsylvania. Thirteen years later, with the development of more advanced techniques, the abnormal chromosome was shown by Janet Rowley to be the result of a translocation of chromosomes 9 and 22. Identification of the ...

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  8. Philadelphia chromosome - Wikipedia

    en.wikipedia.org/wiki/Philadelphia_chromosome

    The chromosomal defect in the Philadelphia chromosome is a reciprocal translocation, in which parts of two chromosomes, 9 and 22, swap places. The result is that a fusion gene is created by juxtaposing the ABL1 gene on chromosome 9 (region q34) to a part of the BCR (breakpoint cluster region) gene on chromosome 22 (region q11).

  9. Oquendo's 20 leads 7 SMU players in double figures ... - AOL

    www.aol.com/oquendos-20-leads-7-smu-033235272.html

    Kario Oquendo hit four 3-pointers and scored 20 points on 7-of-8 shooting Tuesday night to lead seven SMU players scoring in double figures and help the Mustangs beat Alabama State 101-72. Chuck ...

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