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2. X chromosome - Wikipedia

   en.wikipedia.org/wiki/X_chromosome

   CM000685 (FASTA) 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 ...

3. X-linked recessive inheritance - Wikipedia

   en.wikipedia.org/wiki/X-linked_recessive_inheritance

   Second, X-linked recessive traits are more commonly expressed in males than females. [2] This is due to the fact that males possess only a single X chromosome, and therefore require only one mutated X in order to be affected. Women possess two X chromosomes, and thus must receive two of the mutated recessive X chromosomes (one from each parent).

4. Klinefelter syndrome - Wikipedia

   en.wikipedia.org/wiki/Klinefelter_syndrome

   Klinefelter syndrome (KS), also known as 47,XXY, is a chromosome anomaly where a male has an extra X chromosome. [10] These complications commonly include infertility and small, poorly functioning testicles (if present). These symptoms are often noticed only at puberty, although this is one of the most common chromosomal disorders, occurring in ...

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7. Genetic linkage - Wikipedia

   en.wikipedia.org/wiki/Genetic_linkage

   Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart.