Question 1 1 point A human disease appears to be associated

Question 1 (1 point) A human disease appears to be associated with dysfunctional mitochondria, but actually results from a mutation at a single locus in nuclear DNA. This mutation will demonstrate a maternal pattern of inheritance, because mitochondria are passed from female parents to progeny. C paternal pattern of inheritance, because mitochondria are passed from male parents to progeny. non-Mendelian inheritance pattern, because the number of mitochondria varies from cell to cell (and it is impossible to predict how many mitochondria will be passed from parents to offspring). Mendelian inheritance pattern, as the mutation is located on an autosome. None of the above. Save Question 2 (1 point A male Drosophila melanogaster is genotypically e +/e-, where e (ebony) is an autosomal gene. of the four gametes produced during meiosis, how many of these gametes will likely camy both the e- allele and the Y chromosome (assuming that alleles in flies follow Mendel\'s first and second laws)? none 1/4 1/2 3/4 C all of them Save

Solution

1. Mendelian inheritance as mutation is located on autosome.

2.1/4.

3. Chi square Test.

4.