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  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. [5] 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. In humans, there are 23 chromosomes, but ...

  3. Patau syndrome - Wikipedia

    en.wikipedia.org/wiki/Patau_syndrome

    Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13. The extra genetic material disrupts normal development, causing multiple and complex organ defects. This can occur either because each cell contains a full extra copy of chromosome 13 ...

  4. Small supernumerary marker chromosome - Wikipedia

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

    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 be expressed.

  5. USA Gymnastics Says They Have Video Evidence Jordan ... - AOL

    www.aol.com/usa-gymnastics-says-video-evidence...

    In their Aug. 11 statement, USA Gymnastics said they have submitted "time-stamped, video evidence" to the CAS that "shows Landi first stated her request to file an inquiry at the inquiry table 47 ...

  6. Deletion (genetics) - Wikipedia

    en.wikipedia.org/wiki/Deletion_(genetics)

    Deletion on a chromosome. In genetics, a deletion (also called gene deletion, deficiency, or deletion mutation) (sign: Δ) is a mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is left out during DNA replication. Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome. [ 1]

  7. Cri du chat syndrome - Wikipedia

    en.wikipedia.org/wiki/Cri_du_chat_syndrome

    Chromosomal Mutation. Cri du chat syndrome is a rare genetic disorder due to a partial chromosome deletion on chromosome 5. [ 1] Its name is a French term ("cat-cry" or "call of the cat") referring to the characteristic cat-like cry of affected children (sound sample [1] ). [ 2] It was first described by Jérôme Lejeune in 1963. [ 3]

  8. Pallister–Killian syndrome - Wikipedia

    en.wikipedia.org/wiki/Pallister–Killian_syndrome

    The Pallister–Killian syndrome (PKS), also termed tetrasomy 12p mosaicism or the Pallister mosaic aneuploidy syndrome, is an extremely rare and severe genetic disorder. PKS is due to the presence of an extra and abnormal chromosome termed a small supernumerary marker chromosome (sSMC). sSMCs contain copies of genetic material from parts of ...

  9. BET posts ‘unfiltered’ Usher speech after censorship during ...

    www.aol.com/news/bet-posts-unfiltered-usher...

    In the BET video on YouTube, Usher said during one of the parts muted in the live broadcast: "At one point, it got really thick. When mother----- were f---ing with me.

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