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  2. Heredity - Wikipedia

    en.wikipedia.org/wiki/Heredity

    Heredity, also called inheritance or biological inheritance, is the passing on of traits from parents to their offspring; either through asexual reproduction or sexual reproduction, the offspring cells or organisms acquire the genetic information of their parents.

  3. Epigenetics - Wikipedia

    en.wikipedia.org/wiki/Epigenetics

    Epigenetic mechanisms. In biology, epigenetics is the study of heritable traits, or a stable change of cell function, that happen without changes to the DNA sequence. [1] The Greek prefix epi-(ἐπι-"over, outside of, around") in epigenetics implies features that are "on top of" or "in addition to" the traditional (DNA sequence based) genetic mechanism of inheritance. [2]

  4. Hereditary title - Wikipedia

    en.wikipedia.org/wiki/Hereditary_title

    Many other – especially feudal age – offices became inheritable, often connected to military (e.g. keeper of a castle, such as Castellan; in Japan even shōgun) or domanial functions, which is also why some such functions became noble titles (e.g. Burgrave, Margrave). Certain religious positions, such as the Aga Khan and Dā'ī al-Mutlaq.

  5. Inheritance - Wikipedia

    en.wikipedia.org/wiki/Inheritance

    In law, an "heir" (FEM: heiress) is a person who is entitled to receive a share of property from a decedent (a person who died), subject to the rules of inheritance in the jurisdiction where the decedent was a citizen, or where the decedent died or owned property at the time of death.

  6. Gene - Wikipedia

    en.wikipedia.org/wiki/Gene

    In biology, the word gene has two meanings. The Mendelian gene is a basic unit of heredity. The molecular gene is a sequence of nucleotides in DNA that is transcribed to produce a functional RNA. There are two types of molecular genes: protein-coding genes and non-coding genes.

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  9. 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.