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The word pedigree is a corruption of the Anglo-Norman French pé de grue or "crane's foot", either because the typical lines and split lines (each split leading to different offspring of the one parent line) resemble the thin leg and foot of a crane [3] or because such a mark was used to denote succession in pedigree charts. [4] A pedigree ...
Human genetics is the study of inheritance as it ... treatment and help us to understand the genetics of human life. ... identified by pedigree chart analysis ...
In this pedigree chart, G is the progeny of C and F, and C is the biological uncle of F. To find the coefficient of inbreeding of G, first locate a loop that leads from G to the common ancestor through one parent and back down to the other parent without going through the same individual twice.
An ancestry chart, which is a tree showing the ancestors of an individual and not all members of a family, will more closely resemble a tree in shape, being wider at the top than at the bottom. In some ancestry charts, an individual appears on the left and his or her ancestors appear to the right.
An example pedigree chart of an autosomal dominant disorder An example pedigree chart of an autosomal recessive disorder An example pedigree chart of a sex-linked disorder (The gene is on the X chromosome.) The description of a mode of biological inheritance consists of three main categories: 1. Number of involved loci
The Punnett square is a visual representation of Mendelian inheritance, a fundamental concept in genetics discovered by Gregor Mendel. [10] For multiple traits, using the "forked-line method" is typically much easier than the Punnett square.
Mendelian traits behave according to the model of monogenic or simple gene inheritance in which one gene corresponds to one trait. Discrete traits (as opposed to continuously varying traits such as height) with simple Mendelian inheritance patterns are relatively rare in nature, and many of the clearest examples in humans cause disorders.
Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]