For each pedigree shown,

Identify which simple pattern of hereditary transmission (autosomal dominant, autosomal recessive, X-linked dominant, or X-linked recessive) is most likely to have occurred. Give genotypes for individuals involved in transmitting the trait. 

If you knew that a devastating late-onset inherited disease runs in your family (in other words, a disease that does not appear until later in life) and you could be tested for it at the age of 20, would you want to know whether you are a carrier? Would your answer be likely to change when you reach age 40?

The gene causing Coffin–Lowry syndrome (OMIM 303600) was recently identified and mapped on the human X chromosome. Coffin–Lowry syndrome is a rare disorder affecting brain morphology and development. It also produces skeletal and growth abnormalities, as well as abnormalities of motor control. Coffin–Lowry syndrome affects males who inherit a mutation of the X-linked gene. Most carrier females show no symptoms of the disease but a few carriers do. These carrier females are always less severely affected than males. Offer an explanation for this finding.

Four eye-color mutants in Drosophila—apricot, brown, carnation, and purple—are inherited as recessive traits. Red is the dominant wild-type color of fruit-fly eyes. Eight crosses (A through H) are made between parents from pure-breeding lines.

Predict F₂ phenotype ratios of crosses A, B, D, and G.

Four eye-color mutants in Drosophila—apricot, brown, carnation, and purple—are inherited as recessive traits. Red is the dominant wild-type color of fruit-fly eyes. Eight crosses (A through H) are made between parents from pure-breeding lines.

Which of these eye-color mutants are X-linked recessive and which are autosomal recessive? Explain how you distinguish X-linked from autosomal heredity.

The genes encoding the red- and green-color-detecting proteins of the human eye are located next to one another on the X chromosome and probably evolved from a common ancestral pigment gene. The two proteins demonstrate 76 percent homology in their amino acid sequences. A normal-visioned woman (with both genes present on each of her two X chromosomes) has a red-color-blind son who was shown to have one copy of the green-detecting gene and no copies of the red-detecting gene. Devise an explanation for these observations at the chromosomal level (involving meiosis).

The following figure illustrates reciprocal crosses involving chickens with sex-linked dominant barred mutation. For Cross A and for Cross B, cross the F₁ roosters and hens and predict the feather patterns of roosters and hens in the F₂.

A husband and wife have normal vision, although both of their fathers are red–green color-blind, an inherited X-linked recessive condition. What is the probability that their first child will be (a) a normal son, (b) a normal daughter, (c) a color-blind son, (d) a color-blind daughter?

In fruit flies, yellow body (y) is recessive to gray body , and the trait of body color is inherited on the X chromosome. Vestigial wing (v) is recessive to full-sized wing (v⁺), and the trait has autosomal inheritance. A cross of a male with yellow body and full wings to a female with gray body and full wings is made. Based on an analysis of the progeny of the cross shown below, determine the genotypes of parental and progeny flies.

[Table below appears at this point containing crosses and results]