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  2. 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.

  3. DNA² - Wikipedia

    en.wikipedia.org/wiki/DNA²

    Karin receives a new DNA modifier and attempts to shoot Junta, only to miss and hit Ryuji who discovers he has gained the ability to absorb other people's DNA into himself. Using his powers, he morphs into Junta and ruins his reputation with Ami and Tomoko. Afterwards, Ryuji absorbs Junta's powers and defeats him.

  4. DNA2 - Wikipedia

    en.wikipedia.org/wiki/DNA2

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Help; Learn to edit; Community portal; Recent changes; Upload file

  5. List of fictional diseases - Wikipedia

    en.wikipedia.org/wiki/List_of_fictional_diseases

    It starts out with realistic flu symptoms including its first stage being a fever, and then progresses through more fictional nonsensical stages until the infected victim recovers after the seventh (a submissive suggestible stage which Leo insists on being called the "must say yes" stage): "wild rat man" – the infected victim turning feral ...

  6. Partial androgen insensitivity syndrome - Wikipedia

    en.wikipedia.org/wiki/Partial_androgen...

    Approximately one half of all 46,XY individuals born with ambiguous genitalia will not receive a definitive diagnosis. [51] Androgen receptor (AR) gene mutations cannot be found in 27% [6] [32] to 72% [52] of individuals with PAIS. As a result, genetic analysis can be used to confirm a diagnosis of PAIS, but it cannot be used to rule out PAIS. [53]

  7. Haplogroup R-M167 - Wikipedia

    en.wikipedia.org/wiki/Haplogroup_R-M167

    In human genetics, Haplogroup R-M167 (R1b1a1a2a1a2a1b1a1) is a Y-chromosome haplogroup which is a subdivision of Haplogroup R-DF27 and the wider haplogroup R-M269 (more specifically, its subclade R-) defined by the presence of the marker M167 (also known as SRY2627).

  8. Xq28 - Wikipedia

    en.wikipedia.org/wiki/Xq28

    It was concluded that at least one form of male homosexuality is preferentially transmitted through the maternal side and is genetically linked to the Xq28 region. [ 3 ] A follow-up study, Hu et al. (1995), conducted by the Hamer lab in collaboration with two groups of statistical experts in 1995, corroborated the original results for males ...

  9. Disorders of sex development - Wikipedia

    en.wikipedia.org/wiki/Disorders_of_sex_development

    Complete androgen insensitivity syndrome causes a genetic male to have a vagina (often incompletely developed, nearly always blind-ending), breasts, and a clitoris; people with this form are raised as females. [25] Aphallia – a rare condition where a XY male is born without a penis. As of 2017, only 100 cases have been reported in literature ...