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  2. Klinefelter syndrome - Wikipedia

    en.wikipedia.org/wiki/Klinefelter_syndrome

    This XXY chromosome arrangement is one of the most common genetic variations from the XY karyotype, occurring in approximately one in 500 live male births. [4] [14] [37] In mammals with more than one X chromosome, the genes on all but one X chromosome are not expressed; this is known as X inactivation. This happens in XXY males, as well as ...

  3. Trisomy - Wikipedia

    en.wikipedia.org/wiki/Trisomy

    The number of chromosomes in the cell where trisomy occurs is represented as, for example, 2n+1 if one chromosome shows trisomy, 2n+1+1 if two show trisomy, etc. [2] "Full trisomy", also called "primary trisomy", [2] means that an entire extra chromosome has been copied. "Partial trisomy" means that there is an extra copy of part of a chromosome.

  4. Chromosome 2 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_2

    Chromosome 2 is one of the twenty-three pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 2 is the second-largest human chromosome, spanning more than 242 million base pairs [ 4 ] and representing almost eight percent of the total DNA in human cells .

  5. Rare baby born completely in amniotic sac - AOL

    www.aol.com/news/2015-02-25-rare-baby-born...

    A California baby, born prematurely at 26 weeks, is a true rarity. This is 10-week-old Silas Phillips. He was born via cesarean section, completely enclosed in his amniotic sac, something known as ...

  6. Robertsonian translocation - Wikipedia

    en.wikipedia.org/wiki/Robertsonian_translocation

    It is the most common form of chromosomal translocation in humans, affecting 1 out of every 1,000 babies born. [1] It does not usually cause medical problems, though some people may produce gametes with an incorrect number of chromosomes, resulting in a risk of miscarriage. In rare cases this translocation results in Down syndrome and Patau ...

  7. Triploid syndrome - Wikipedia

    en.wikipedia.org/wiki/Triploid_syndrome

    Triploidy can result from either two sperm fertilizing one egg (60%) or from one sperm fertilizing an egg with two copies of every chromosome (40%). [2] These are otherwise known as diandric fertilization and digynic fertilization. Pregnancies caused by digynic fertilization are more likely to end right before a baby is due for full term.

  8. XXYY syndrome - Wikipedia

    en.wikipedia.org/wiki/XXYY_syndrome

    48,XXYY syndrome is a condition related to the X and Y chromosomes (the sex chromosomes). People normally have 46 chromosomes in each cell.Two of the 46 chromosomes, known as X and Y, are called sex chromosomes because they help determine whether a person will develop male or female sex characteristics.

  9. Another Baby Was Born With the DNA From 3 People - AOL

    www.aol.com/lifestyle/another-baby-born-dna-3...

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