A population has the following data: Genotype Number AA 65 Aa aa 25 Convert the frequency from Question 1g (the expected frequency of Aa) into total number of people with Aa O 79 59 O 69 89
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- Edio | Calendar X Edio | Student Da x days/1089977/lessons/1533969/variants/2439102/take/10/ A Q TEXT ANSWER The inheritance patterns for some traits in guinea pigs are listed in the table below. 1. Identify the phenotype of a guinea pig with the genotype HhBBrr. 2. Using the allele symbols in the table, identify the genotype of a guinea pig that is recessive for hair length, heterozygous for hair color, and homozygous dominant for hair texture. Trait Dominant Allele Recessive Allele hair short (H) long (h) length hair color black (B) white (b) rough (R) smooth (r) hair texture BIUG X₁ X¹ EEAA H Normal : √x Enter your answer here ŏooooo Questions Answered 中山川 Ω Ο Τ Edio | Calendar X RepostExchange X Practice All Changes Saved ContinueI need help in table 2 & 3 please Table 1 Phenotype O E O-E (O-E)^2 (O-E)^2 /E Disease, Male 304 433.875 129.875 16789.68 38.69 Disease, Female 267 433.875 166.875 26855.01 61.89 WT, Male 285 144.625 140.375 19705.14 136.25 WT, Female 301 144.625 156.375 24453.15 156.37 Total 1157 1157 393.20 DF 3 p-value 7.84 Expected progencies as per SLR MOI’s = 1:1 for both male and female Phenotype O E O-E (O-E)^2 (O-E)^2 /E Disease, Male 304 289.25 14.75 217.56 0.75 Disease, Female 267 289.25 22.25 495.06 1.85 WT, Male 285 289.25 4.25 18.06 0.06 WT, Female 301 289.25 11.75 138.06 0.46 Total 1157 1157 3.12 DF 3 p-value 7.84 Progenies are following SR MOI’s that parents have genotypes and progenies in ratio 1:1 In Table 2,…I Review Lesch-Nyhan syndrome (OMIM 300322) is a rare X-linked recessive disorder that produces severe mental retardation, spastic cerebral palsy, and self- mutilation. Part A What is the probability that the first son of a woman whose brother has Lesch-Nyhan syndrome will be affected? Express your answer as a fraction (example 1/16). Submit Request Answer Part B If the first son of the woman described in (a) is affected, what is the probability that her second son is affected? Express your answer as a fraction (example 1/16). Submit Request Answer
- I'm stuck on A1. Question what notation would you use to characterize patient a's karyotype? I put 45, xx/xy +13 but I'm not sure>> Remaining Time: 25 minutes, 51 seconds. * Question Completion Status: L Unce started, this test must be completed in one sitting. Do not le Your answers are saved automatically. 20 Question 4 O 4 5 6 7 8 A Moving to another question will save this response. 9 Which example does not directly support the good gene hypothesis? peacocks with larger eyespots have babies with higher survival rates female (peahens) prefer male (peacocks) with long tail feathers a male peacock with more of eye spots has larger babies peacocks with more ornaments on their tails were less likely to be eaten by a fox 10 11 12 13 A Moving to another question will save this response.E- Question 1/18 NEXT A BOOKMARK Previous Scenario 1: A man and woman have decided to have children but are worried about possible genetic diseases. The couple visits a geneticist to determine what the possible risks are for their future children. The couple discovers that the mom is a carrier, or heterozygous with the diabetes allele and the dad is homozygous dominant, so neither of them have the disease but the mom has one recessive allele. In order to have Diabetes, you have to have two recessive alleles. The following year, the parents are blessed with a bouncing baby boy! What is the correct genotype of the mom? Aa AA aa
- ab H Q9. Who's gonna take you home tonight? There has been a mix up in the maternity ward. The babies have managed to remove their wrist bands. On their wrist bands are their blood groups and names. and art Billy Smith Blood group:A Sarah Chadwick Blood group:AB Imran Ahmed Blood group:B Johnny Honest Blood group:0 nislax 80 Complete the table to match each parent to their baby by indicating the parental genotypes using the symbols IA, IB, and i, and then the name of the baby that belongs to each set of moo parents. Consider one blood type might have more than one genotype. ever Parental Blood groups Parents Genotype Baby Blood Group O and O si grappo AB and O 196² A and O AB and A Completed forms to be made available for external moderation.Trivla Game Show _Make Your Own Tri ngston.schoology.com/common-assessment-delivery/start/4789189591?action=onresume&submissionld=463322566 Dillon WF g Aa v Done In guinea pigs, black hair (B) is dominant to white hair (b) and rough hair (R) is dominant to smooth hair (r). What are all the possible genotypes of a guinea pig that has black, rough hair? (Select all that apply.) O BBRR BBRr BBrr BBRR BbRr O bbRR O bbRr O bbrr O Black O White O Rough OSmooth O Rough O Smoothquestions below: Aura and Ryan are expecting a child. Aura has dark eyes and Ryan has light eyes. Aura's mother has light eyes. Draw a Punnett square and be sure to include the following information for full credit: 1. Place the parents alleles at the top and on the left side. 2. Write in the allele crosses inside the Punnett squares. 3. Write out the genotypes probabilities for an offspring. 4. Write out the phenotype probabilities for an offspring. 5. What is the probability that Aura and Ryan could have a child with light eyes, even if light is recessive to dark? Note: For this question, you will have to go further back into the family tree to get Aura's genotype.
- Question 5 2 pts The genotype for a homozygous Type O person is 00 IAi IBi Question 6 2 pts A woman who is heterozygous for hemophilia has a child with a man who is normal clotting blood. Could they have a hemophiliac child? yes O No answer text provided. No answer text provided. O noWith multiple alleles, there can be more than two genetic alternatives for a given locus. True False Submit Request Answer Provide Feedback m/myct/itemView?assignment ProblemID=10436480&offset=next MacBook ProUse keyboard only to enter your answer below. ALL WORKING MUST BE SHOWN Problem 1) mutation in a gene on chromosome 15 that codes for an enzyme. The disease is an inherited autosomal recessive condition which is Tay-Sachs disease is caused by loss of function found amongst Ashkenazi Jews of Central European origin. In this population, 3 in 5,200 children are born with the disease. What proportion of the population are carriers (heterozygotes) for this disease?