The accompanying pedigree shows the transmission of albinism (absence of skin pigment) in a human family.

What is the probability that female I-3 is a heterozygous carrier of the allele for albinism? 

Nail–patella syndrome is an autosomal disorder affecting the shape of nails on fingers and toes as well as the structure of kneecaps. The pedigree below shows the transmission of nail–patella syndrome in a family along with ABO blood type.

Explain why III-6 has nail–patella syndrome and III-8 does not. Give genotypes for these two individuals.

Nail–patella syndrome is an autosomal disorder affecting the shape of nails on fingers and toes as well as the structure of kneecaps. The pedigree below shows the transmission of nail–patella syndrome in a family along with ABO blood type.

Using N and n to represent alleles at the nail–patella locus and Iᴬ, Iᴮ and i to represent ABO alleles, write the genotypes of I-1 and I-2 as well as their five children in generation II.

Consider this human pedigree for a vision defect.

What is the most probable mode of inheritance of the disease? Identify any discrepancies between the pedigree and your proposed mode of transmission, and provide possible explanations for these exceptions. 

The accompanying pedigree shows the transmission of albinism (absence of skin pigment) in a human family.

One child of female I-3 has albinism. What is the probability that any of the other four children are carriers of the allele for albinism? 

The accompanying pedigree shows the transmission of albinism (absence of skin pigment) in a human family.

The female I-1 and her mate, male I-2, had four children, one of whom has albinism. What is the probability that they could have had a total of four children with any other outcome except one child with albinism and three with normal pigmentation? 

The accompanying pedigree shows the transmission of albinism (absence of skin pigment) in a human family.

Using allelic symbols of your choice, identify the genotypes of the male and his two mates in generation I. 

The accompanying pedigree shows the transmission of albinism (absence of skin pigment) in a human family.

What is the most likely mode of transmission of albinism in this family? 

Thalassemia is an inherited anemic disorder in humans. Affected individuals exhibit either a minor anemia or a major anemia. Assuming that only a single gene pair and two alleles are involved in the inheritance of these conditions, is thalassemia a dominant or recessive disorder?