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  2. Distal 18q- - Wikipedia

    en.wikipedia.org/wiki/Distal_18q-

    Specialty. Medical genetics. Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. [1] The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18. [2]

  3. Proximal 18q- - Wikipedia

    en.wikipedia.org/wiki/Proximal_18q-

    Proximal 18q-is a rare genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. This deletion involves the proximal (near the centromere ) section of the long arm of chromosome 18 somewhere between 18q11.2 (18.9 Mb) to 18q21.1 (43.8 Mb). [1]

  4. Trisomy 18 - Wikipedia

    en.wikipedia.org/wiki/Trisomy_18

    1 per 5,000 births [3] Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [3] Many parts of the body are affected. [3] Babies are often born small and have heart defects. [3] Other features include a small head, small jaw, clenched fists with overlapping ...

  5. Chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_18

    CM000680 ( FASTA) Chromosome 18 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of DNA) and represents about 2.5 percent of the total DNA in cells .

  6. 18p- - Wikipedia

    en.wikipedia.org/wiki/18p-

    18p-. 18p-, also known as monosomy 18p, deletion 18p syndrome, del (18p) syndrome, partial monosomy 18p, or de Grouchy syndrome 1, is a genetic condition caused by a deletion of all or part of the short arm (the p arm) of chromosome 18. It occurs in about 1 of every 50,000 births. [ 1 ]

  7. Ring chromosome 18 - Wikipedia

    en.wikipedia.org/wiki/Ring_chromosome_18

    Individuals with ring 18 have one of their two copies of chromosome 18 that has formed the shape of a ring. The ring is formed when the caps on both the long arm (q) and the short arm (p) of one copy of chromosome 18 are lost and the new ends re-join to form the ring. Because the ring involves deletions of both the long arm (18q-) and the short ...

  8. Smith–Magenis syndrome - Wikipedia

    en.wikipedia.org/wiki/Smith–Magenis_syndrome

    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. Dogs don't actually age 7 times faster than humans, new ... - AOL

    www.aol.com/lifestyle/dogs-dont-actually-age-7...

    Say you have a 4-year-old Labrador named Comet — with the new equation, Comet's real "dog age" would be slightly older than 53. The reason for the difference is actually pretty simple.