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  2. Chromosome 12 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_12

    Chromosome 12 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. People normally have two copies of this chromosome. Chromosome 12 spans about 133 million base pairs (the building material of DNA ) and represents between 4 and 4.5 percent of the total DNA in cells .

  3. Genetics - Wikipedia

    en.wikipedia.org/wiki/Genetics

    Genetics is the study of genes, genetic variation, and heredity in organisms. [ 1 ] [ 2 ] [ 3 ] It is an important branch in biology because heredity is vital to organisms' evolution . Gregor Mendel , a Moravian Augustinian friar working in the 19th century in Brno , was the first to study genetics scientifically.

  4. Hardy–Weinberg principle - Wikipedia

    en.wikipedia.org/wiki/Hardy–Weinberg_principle

    In population genetics, the Hardy–Weinberg principle, also known as the Hardy–Weinberg equilibrium, model, theorem, or law, states that allele and genotype frequencies in a population will remain constant from generation to generation in the absence of other evolutionary influences.

  5. Genetics for Beginners - Wikipedia

    en.wikipedia.org/wiki/Genetics_for_Beginners

    Genetics for Beginners, republished as Introducing Genetics, is a 1993 graphic study guide to Genetics written by Steve Jones and illustrated by Borin Van Loon.The volume, according to the publisher's website, "takes readers on a journey through this new science to the discovery of DNA and the heart of the human gene map," and, "gives us the information," to, "make moral decisions where ...

  6. Consanguinity - Wikipedia

    en.wikipedia.org/wiki/Consanguinity

    In clinical genetics, consanguinity is defined as a union between two individuals who are related as second cousins or closer, with the inbreeding coefficient (F) equal or higher than 0.0156, where (F) represents the proportion of genetic loci at which the child of a consanguineous couple might inherit identical gene copies from both parents. [25]

  7. Maternal effect - Wikipedia

    en.wikipedia.org/wiki/Maternal_effect

    In genetics, a maternal effect occurs when the phenotype of an organism is determined by the genotype of its mother. [1] For example, if a mutation is maternal effect recessive, then a female homozygous for the mutation may appear phenotypically normal, however her offspring will show the mutant phenotype, even if they are heterozygous for the mutation.

  8. 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.

  9. Chromosomal inversion - Wikipedia

    en.wikipedia.org/wiki/Chromosomal_inversion

    An inversion is a chromosome rearrangement in which a segment of a chromosome becomes inverted within its original position. An inversion occurs when a chromosome undergoes a two breaks within the chromosomal arm, and the segment between the two breaks inserts itself in the opposite direction in the same chromosome arm.