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If individuals 1 and 2 marry what is probability that their first child will have the kidney disease?
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- 1) What is the pure-breeding (or true-breeding) strain or organism?Figure 7.2 If a mutation occurs so that a fungus is no longer able to produce a minus mating type, will it still be able to reproduce? Figure 7.2 (a) In animals, sexually reproducing adults form haploid gametes from diploid germ cells. (b) Fungi, such as black bread mold (Rhizopus nigricans), have haploid-dominant life cycles. (c) Plants have a life cycle that alternates between a multicellular haploid organism and a multicellular diploid organism. (credit c fern: modification of work by Cory Zanker; credit c gametophyte: modification of work by Vlmastra/Wikimedia Commons)d/1n5NtidRwTwUzcDkDPi5Z9P SHPZ9IA-XH-pfftLbhNc/edit 1) @ Is Add-ons Help Last edit was 15 minutes ago | Calibri в I UA 12 + 3I | II 6 1 I 7. Construct a Punnett square for a cross between two heterozygous pea plants with violet flower color. a. What genotypes would you expect in the offspring? b. What percentage or ratio of each genotype would you expect in the offspring? !!!
- the offspring ès) can often be autosomal I 1.1 III ad amalg od no IV 9 OTO 5 0000 anivellor and goje If individual 2 were to marry a woman with no family history of the disease, which of the following would most likely be true of their children? a. All of the children would have the disease. b. None of the children would have the disease. c. Only the sons would have the disease. d. All of the sons would be carriers of the disease. e. None of the daughters would be carriers of the disease.Is cystic fibrosis a genotypic or phenotypic change? Explain your reasoning. Edit View Insert Format Tools Table, 12pt v Paragraph BIU A 2 T?くA young couple went to see a genetic counselor because each had a sibling with cystic fibrosis. (Cysticfibrosis is a recessive disease, and neither member ofthe couple nor any of their four parents is affected.)a. What is the probability that the female of thiscouple is a carrier?b. What are the chances that their child will havecystic fibrosis?c. What is the probability that their child will be acarrier of the cystic fibrosis disease allele?
- Which of the karyotypes shown is from a normal female?Identify the sex and any genetic conditions of this individual by analyzing the karyotype. 1. female or male? 2. normal, triploid, patau, edwards syndrom, down syndrom, triplo-X, turners syndrom, or klinifelter syndrom?2 3 4 5 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 ху Which chromosome set has an extra What diagnosis would you give this patient?. Finish the notation for this patient's karyotype: What causes a dark band on the chromosome? What is a centromere?
- ESHANEL X E Edulastic X SHANEIL X - AttendaX A Do Now x O Genetics x A Codomi X Codom X Ô https://www.liveworksheets.com/oq1336503xg Homozygous or Heterozygous 1. Bb 2. FF 3. DD 4. Rr Genotypes and Phenotypes 5. Tt 6. Qq 7. Long nose 8. HH 9. Brown hair Punnett Square B = Purple Hair b = Yellow Hair %3D97 Assume that the trihybrid cross MM SS tt X mm ss TT is made in a plant species in which Mand S are dom- inant but there is no dominance between T and t. Consider the F2 progeny from this cross, and assume independent assortment. (a) How many phenotypic classes are expected? (b) What is the probability of genotype MM SS t? obib (c) What proportion would be expected to be 15 2nod bolleo homozygous for all genes? ablla Insninmobo.(omConsider this pedigree showing an autosomal dominant rare disorder. What is the degree of penetrance? Show your work. na оп 16 19 fa 16 R 9X