Answer(4)(a)1
please show work 4. The pedigree shown at below is for a rare autosomal recessive trait....
A pedigree affected by a rare human autosomal recessive trait is shown below. ODO What is the probability that III-2 is a carrier? (enter your answer as a percentage; if the answer is 83% enter 83) Answer:
Given the pedigree below for a rare autosomal trait, what is the likelihood that Persons A and B would have an affected child? 60p on Select one: O a. 1/72 b. 1/48 O O C 1/144 d. 1/96 e. 1/16
If the pedigree shown is for an autosomal recessive trait, what are the genotypes of individuals II-1, II-6 and II-9, where A- is not kooky and aa is kooky. | 11 2 3 Ooh 14 5 6
QUESTION 9 5 pe If the characteristic depicted in the pedigree below is rare and subject to complete penetrance, it is likely to be X-linked recessive? 5 6 7 -OOO No, because individuals ll-2 and 11-4 are not affected No, because individuals 111-4 and III-6 are not affected Yes, because individuals III-4 and III-6 are not affected Yes, because only females are affected in generation 11 1. The gene for cystic fibrosis (normal dominant allele CF and abnormal recessive allele...
For the following pedigree (Pedigree Tree I, used for following questions, too), decide whether a trait is inherited as an autosomal dominant, autosomal recessive, or X-linked recessive. 2 10 11 po og po 0000 TO 1 2 3 4 5 12 13 14 Autosomal dominant Most likely autosomal recessive Most likely X-linked recessive Autosomal recessive X-linked recessive Either autosomal recessive or X-linked recessive QUESTION 4 (Pedigree Tree 1) What is the genotype of Generation individual 12 АА ОАа Оаа Either...
The given image shows the pedigree of a family with an autosomal recessive disorder. Analyze the pedigree to determine the probability of individual 12 being a carrier. Please write your answer as a probability from 0 to 1. Probability:
1. In the pedigree below, the shaded in portions represent an albino (recessive trait). Determine the genotypes of each numbered individual and write them next to each individual. Use the letters A and a to describe the genotype and then also use the terminology homozygous dominant, heterozygous, homozygous recessive. Use a - when the second allele is no known. cho
Genetics problem! Alkaptonuria is a rare recessive disorder that causes urine to turn black when exposed to air and is caused by a mutation in the homogentisate 1.2-dioxygenase (HGD) gene. Examine the pedigree below and answer the questions. What is the probability that individual A is heterozygous? What is the probability that individual B is heterozygous?
What is the mode of inheritance for hypercholesterolemia? a. Autosomal dominant b. Autosomal recessive c. X-linked dominant d. X-linked recessive e. More than one of the above are possible ---------------------------------------------------------------- What is the mode of inheritance for Hunter's syndrome? a. Autosomal dominant b. Autosomal recessive c. X-linked dominant d. X-linked recessive e. More than one of the above are possible. ------------------------------------------------------------ What is the genotype for individual II-3 at the hypercholesterolemia locus (dominant allele is denoted by H, recessive allele...
Examine the pedigree chart below: Is the trait inherited as a dominant or a recessive trait? [Note: the trait is an autosomal trait]. Explain your reasoning. Diagram source: France, D. (2001). Lab Manual and Workbook for Physical Anthropology (4th Ed). Wadsworth Thomson Learning Publishing Co.