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  2. Sex linkage - Wikipedia

    en.wikipedia.org/wiki/Sex_linkage

    Sex linked describes the sex-specific reading patterns of inheritance and presentation when a gene mutation is present on a sex chromosome (allosome) rather than a non-sex chromosome . In humans, these are termed X-linked recessive, X-linked dominant and Y-linked. The inheritance and presentation of all three differ depending on the sex of both ...

  3. Chromosome 5 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_5

    Chromosome 5 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 5 spans about 182 million base pairs (the building blocks of DNA) and represents almost 6% of the total DNA in cells. Chromosome 5 is the 5th largest human chromosome, yet has one of the lowest gene densities.

  4. Sexual differentiation in humans - Wikipedia

    en.wikipedia.org/wiki/Sexual_differentiation_in...

    Most mammals, including humans, have an XY sex-determination system: the Y chromosome carries factors responsible for triggering male development. In the absence of a Y chromosome, the fetus will undergo female development. This is because of the presence of the sex-determining region of the Y chromosome, also known as the SRY gene. [5]

  5. Sex-determination system - Wikipedia

    en.wikipedia.org/wiki/Sex-determination_system

    The sex-chromosome turnover is an evolutionary phenomenon where sex chromosomes disappear, or becomes autosomal, and autosomal chromosomes become sexual, repeatedly over evolutionary time. Some lineages have extensive turnover, but others don't.

  6. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    The basic number of chromosomes in the somatic cells of an individual or a species is called the somatic number and is designated 2n. In the germ-line (the sex cells) the chromosome number is n (humans: n = 23). [4] [5] p28 Thus, in humans 2n = 46. So, in normal diploid organisms, autosomal chromosomes are present in two copies.

  7. Chromosomal rearrangement - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_rearrangement

    It shows 22 homologous autosomal chromosome pairs, both the female (XX) and male (XY) versions of the two sex chromosomes, as well as the mitochondrial genome (at bottom left). In genetics, a chromosomal rearrangement is a mutation that is a type of chromosome abnormality involving a change in the structure of the native chromosome. [1]

  8. Genetic diagnosis of intersex - Wikipedia

    en.wikipedia.org/wiki/Genetic_diagnosis_of_intersex

    [14] [5] These include 5-alpha-reductase deficiency and androgen insensitivity syndrome, traits evident in elite Olympic-level women athletes and "the world's first openly intersex mayor". [14] [15] In 2015, the Council of Europe published an Issue Paper on Human rights and intersex people, remarking on a right to life:

  9. Sex differences in psychology - Wikipedia

    en.wikipedia.org/wiki/Sex_differences_in_psychology

    Biological differentiation is a fundamental part of human reproduction. Generally, males have two different sex chromosomes, an X and a Y; females have two X chromosomes. The Y chromosome, or more precisely the SRY gene located on it, is what generally determines sexual differentiation. If a Y chromosome with an SRY gene is present, growth is ...