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  2. Achondroplasia - Wikipedia

    en.wikipedia.org/wiki/Achondroplasia

    About 80% of cases occur in children of parents without the disease, and result from a new (de novo, or sporadic) mutation, which most commonly originates as a spontaneous change during spermatogenesis. [5] The rest are inherited from a parent with the condition. [3] The risk of a new mutation increases with the age of the father. [4]

  3. Genetically modified fish - Wikipedia

    en.wikipedia.org/wiki/Genetically_modified_fish

    Genetically modified fish (GM fish) are organisms from the taxonomic clade which includes the classes Agnatha (jawless fish), Chondrichthyes (cartilaginous fish) and Osteichthyes (bony fish) whose genetic material has been altered using genetic engineering techniques.

  4. Fish reproduction - Wikipedia

    en.wikipedia.org/wiki/Fish_reproduction

    As with all types of asexual reproduction, there are both costs (low genetic diversity and therefore susceptibility to adverse mutations that might occur) and benefits (reproduction without the need for a male) associated with parthenogenesis. Parthenogenesis in sharks has been confirmed in the bonnethead [35] and zebra shark. [36]

  5. 50 Of The Wildest And Cutest Genetic Mutations Ever ... - AOL

    www.aol.com/111-rarest-genetic-mutations-ever...

    While genetic mutations occur naturally in the wild, some breeders have come under fire for purposely creating “mutant” animals. In 2015, some South African breeders and ranchers made ...

  6. Compound heterozygosity - Wikipedia

    en.wikipedia.org/wiki/Compound_heterozygosity

    In medical genetics, compound heterozygosity is the condition of having two or more heterogeneous recessive alleles at a particular locus that can cause genetic disease in a heterozygous state; that is, an organism is a compound heterozygote when it has two recessive alleles for the same gene, but with those two alleles being different from each other (for example, both alleles might be ...

  7. Trimethylaminuria - Wikipedia

    en.wikipedia.org/wiki/Trimethylaminuria

    [6] [7] [8] Loss-of-function mutations, nonsense mutations, and missense mutations are three of the most common. Nonsense and missense mutations cause the most severe phenotypes. [citation needed] In 2007 the evolution of the FMO3 gene was studied, including the evolution of some mutations associated with TMAU. [9]

  8. Tiffani Thiessen Shares Her Hopes for Upcoming “White ... - AOL

    www.aol.com/tiffani-thiessen-shares-her-hopes...

    White Collar may be back sooner than you think!. Tiffani Thiessen tells PEOPLE exclusively she hopes the anticipated revival of the police procedural gets turned around "pretty fast.". The actress ...

  9. Bateson–Dobzhansky–Muller model - Wikipedia

    en.wikipedia.org/wiki/Bateson–Dobzhansky...

    The Dobzhansky–Muller incompatibilities can result from purely random, neutral or non-selected differences between the populations. They can also be driven by natural selection in at least two ways. When two populations diverge from each other and encounter new - and different - environments they may adapt to these environments.