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  2. Polyploidy - Wikipedia

    en.wikipedia.org/wiki/Polyploidy

    Polyploidy is a condition in which the cells of an organism have more than two paired sets of chromosomes. Most species whose cells have nuclei ( eukaryotes ) are diploid , meaning they have two complete sets of chromosomes, one from each of two parents; each set contains the same number of chromosomes, and the chromosomes are joined in pairs ...

  3. Chimera (genetics) - Wikipedia

    en.wikipedia.org/wiki/Chimera_(genetics)

    The term genetic chimera has been used at least since the 1944 article of Belgovskii. [32] This condition is either innate or it is synthetic, acquired for example through the infusion of allogeneic blood cells during transplantation or transfusion. [citation needed] In nonidentical twins, innate chimerism occurs by means of blood vessel ...

  4. Leucism - Wikipedia

    en.wikipedia.org/wiki/Leucism

    Leucism (/ ˈ l uː s ɪ z əm,-k ɪ z-/) [2] [3] [4] is a wide variety of conditions that result in partial loss of pigmentation in an animal—causing white, pale, or patchy coloration of the skin, hair, feathers, scales, or cuticles, but not the eyes. [4] It is occasionally spelled leukism.

  5. Mosaic (genetics) - Wikipedia

    en.wikipedia.org/wiki/Mosaic_(genetics)

    An example of this is one of the milder forms of Klinefelter syndrome, called 46,XY/47,XXY mosaic wherein some of the patient's cells contain XY chromosomes, and some contain XXY chromosomes. The 46/47 annotation indicates that the XY cells have the normal number of 46 total chromosomes, and the XXY cells have a total of 47 chromosomes.

  6. List of genetic disorders - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_disorders

    The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.

  7. Mutation - Wikipedia

    en.wikipedia.org/wiki/Mutation

    With recents advancements in next-generation sequencing (NGS), all types of de novo mutations within the genome can be directly studied, the detection of which provides a magnitude of insight toward the causes of both rare and common genetic disorders. Currently, the best estimate of the average human germline SNV mutation rate is 1.18 x 10^-8 ...

  8. Pleiotropy - Wikipedia

    en.wikipedia.org/wiki/Pleiotropy

    Similar predictors exist for plant and animal species and are used in agricultural breeding. One measure of pleiotropy is the fraction of genetic variance that is common between two distinct complex human traits: e.g., height vs bone density, breast cancer vs heart attack risk, or diabetes vs hypothyroidism risk.

  9. Outline of genetics - Wikipedia

    en.wikipedia.org/wiki/Outline_of_genetics

    The following outline is provided as an overview of and topical guide to genetics: . Genetics – science of genes, heredity, and variation in living organisms. [1] [2] Genetics deals with the molecular structure and function of genes, and gene behavior in context of a cell or organism (e.g. dominance and epigenetics), patterns of inheritance from parent to offspring, and gene distribution ...