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  2. XY sex-determination system - Wikipedia

    en.wikipedia.org/wiki/XY_sex-determination_system

    Offspring have two sex chromosomes: an offspring with two X chromosomes (XX) will develop female characteristics, and an offspring with an X and a Y chromosome (XY) will develop male characteristics, except in various exceptions such as individuals with Swyer syndrome, that have XY chromosomes and a female phenotype, and de la Chapelle Syndrome ...

  3. Sexual differentiation in humans - Wikipedia

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

    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] Thus, male mammals typically have an X and a Y chromosome (XY), while female mammals typically have two X chromosomes (XX).

  4. XX male syndrome - Wikipedia

    en.wikipedia.org/wiki/XX_male_syndrome

    The tip of the Y chromosome contains the SRY gene and, during recombination, a translocation occurs in which the SRY gene becomes part of the X chromosome. [15] [26] If a fetus is conceived from a sperm cell with an X chromosome bearing the SRY gene, it will develop as a male despite not having a Y chromosome. This form of the condition is ...

  5. Parthenogenesis - Wikipedia

    en.wikipedia.org/wiki/Parthenogenesis

    In species that use the XY sex-determination system, parthenogenetic offspring have two X chromosomes and are female. In species that use the ZW sex-determination system the offspring genotype may be one of ZW (female), [28] [29] ZZ (male), or WW (non-viable in most species, [31] but a fertile, [dubious – discuss] viable female in a few, e.g ...

  6. Sex-determination system - Wikipedia

    en.wikipedia.org/wiki/Sex-determination_system

    The nematode C. elegans is male with one sex chromosome (X0); with a pair of chromosomes (XX) it is a hermaphrodite. [22] Its main sex gene is XOL, which encodes XOL-1 and also controls the expression of the genes TRA-2 and HER-1. These genes reduce male gene activation and increase it, respectively. [23]

  7. XY gonadal dysgenesis - Wikipedia

    en.wikipedia.org/wiki/XY_gonadal_dysgenesis

    XY complete gonadal dysgenesis, also known as Swyer syndrome, is a type of defect hypogonadism in a person whose karyotype is 46,XY. Though they typically have normal vulvas, [1] the person has underdeveloped gonads, fibrous tissue termed "streak gonads", and if left untreated, will not experience puberty.

  8. Parthenogenesis in squamates - Wikipedia

    en.wikipedia.org/wiki/Parthenogenesis_in_squamates

    Parthenogenesis is a mode of asexual reproduction in which offspring are produced by females without the genetic contribution of a male. Among all the sexual vertebrates, the only examples of true parthenogenesis, in which all-female populations reproduce without the involvement of males, are found in squamate reptiles (snakes and lizards). [1]

  9. Sex differences in humans - Wikipedia

    en.wikipedia.org/wiki/Sex_differences_in_humans

    Females normally have two X chromosomes while males typically have an X and a Y chromosome. The X chromosome is more active and encodes more information than the Y chromosome, which has been shown to affect behavior. [14] Genetic researchers theorize that the X chromosome may contain a gene influencing social behaviours. [15] [better source needed]