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2. Xp11.2 duplication - Wikipedia

   en.wikipedia.org/wiki/Xp11.2_Duplication

   Xp11.2 duplication is a genomic variation marked by the duplication of an X chromosome region on the short arm p at position 11.2, defined by standard karyotyping ( G-banding ). This gene-rich, rearrangement prone region can be further divided into three loci - Xp11.21, Xp11.22 and Xp11.23. The duplication could involve any combination of these ...

3. X chromosome - Wikipedia

   en.wikipedia.org/wiki/X_chromosome

   The X chromosome is one of the two sex chromosomes in many organisms, including mammals, and is found in both males and females. It is a part of the XY sex-determination system and XO sex-determination system. The X chromosome was named for its unique properties by early researchers, which resulted in the naming of its counterpart Y chromosome ...

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   These Basic Earbuds. The Work Earbuds Classic. Raycon. For everyday wear that’s easy to take in and out, these buds are the perfect pick! See it! Get The Work Earbuds Classic (originally $120 ...

5. Comparison of English dictionaries - Wikipedia

   en.wikipedia.org/wiki/Comparison_of_English...

   This is a comparison of English dictionaries, which are dictionaries about the language of English.The dictionaries listed here are categorized into "full-size" dictionaries (which extensively cover the language, and are targeted to native speakers), "collegiate" (which are smaller, and often contain other biographical or geographical information useful to college students), and "learner's ...

6. XYY syndrome - Wikipedia

   en.wikipedia.org/wiki/XYY_syndrome

   Frequency. ~1 in 1,000 males [1] XYY syndrome, also known as Jacobs syndrome, is an aneuploid genetic condition in which a male has an extra Y chromosome. [1] There are usually few symptoms. [2] These may include being taller than average and an increased risk of learning disabilities.

7. Robertsonian translocation - Wikipedia

   en.wikipedia.org/wiki/Robertsonian_translocation

   Robertsonian translocation ( ROB) is a chromosomal abnormality where the entire long arms of two different chromosomes become fused to each other. 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 ...