• Consider the selfed offspring of a AaBbCcDd individual: •What is the probability that offspring will have the following genotypes: • AABBCCDD • AaBbCCDd - A_B_C_D_ BbCCDd 1/4 x 1/4 x 1/4 x 1/4= 1/256 1/2 x 1/2 x 1/4 x 1/2= 1/32 3/4 x 3/4 x 3/4 x 3/4= 81/256 1 x 1/2 x 1/4 x 1/2= 1/16 - Same genotype as the parent? - Same phenotype as the parent?
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- A research team interested in mapping human genes discovered a new restriction length polymorphism (RFLP). a. First, they test the RFLP in a family with the pedigree below. The individuals colored blue are affected by hemophelia, a blood clotting disease. Dad Mom daughter1 daughter2 son1 son1 On what chromosome is the RFLP found? Explain your answer. b. Next, they genotyped (determined the RFLP polymorphism, type 1 or type 2) of daughterl's family with the results shown below: husband daughter1 %3D Are the RFLP and the hemophilia gene linked? Explain your reasoning.E Samu E Samu FAIPQLSCDH_No2]MEaHUdrt5NWa2uY6AaKa7Bhy4xfhwplF-CsVAbyA/formResponse Gmail YouTube O Maps Which model below accurately depicts the process of mitosis? * 2n 2n 2n Option 1 Option 2 2n 2n 2n 2n Option 4 Option 3Please ASAP. Thank you. The following diagram represents the results of hemoglobin samples of 5 patients (1-5) that were run on an electrophoresis gel at pH 9.2. The first 3 lanes show the control samples, for comparison. Consider Patient 4 and Patient 5. If patient 4 is female and patient 5 is a male, and they conceive a child together, is there a good chance that the child will have sickle cell anemia (the disease)? Answer Yes or No
- d/e/1FAIPQLSCDH_No2]MEaHUdrt5NWa2uY6AaKa7Bhy4xfhwplF-CsVAbyA/formResponse M Gmail YouTube O Maps Which phrase best describes a human with the chromosomes represented in the karyotype below? * 1 3 4 5 X r8 K* XX从 6. 8 9. 10 X* ** ** 11 12 13 14 15 16 17 18 19 20 XX 44 21 22 XX O A female who exhibits Down syndrome A male who exhibits Down syndrome O A female who does not exhibit Down syndrome O A male who does not exhibit Down syndrome 8.Please ASAP. Thank you. The following diagram represents the results of hemoglobin samples of 5 patients (1-5) that were run on an electrophoresis gel at pH 9.2. The first 3 lanes show the control samples, for comparison. Consider Patient 4 and Patient 5. If patient 2 is female and patient 5 is a male, and they conceive a child together, what is the chance that the child will have sickle cell anemia (the disease)? Give your answer as a percentage (%)Genotype HA На hA ha НА НН АА НН Аа Hh AA Hh Aa На НН Аа НН аа Hh Аа Hh aa hA Hh AA Hh Aa hh AA hh Aa ha Hh Aa Hh aa hh Aa hh aa Key: H = long hair h = short hair A = brown a = green What is the probability that the fırst offspring will be either long-haired and brown-eyed or long- haired and green-eyed? 80% O5% 25% 50%
- Pedigree Analysis Examine the following pedigrees. 1 Examine the pedigree of achondroplasia (a form of dwarfism). a Is this trait dominant or recessive? b How do you know? c Label all of the genotypes on the pedigree chart. II Laboratory Exercise 9 Trait Genetics 113 %3D2: Chart v Add-ins Media Links Comment Footer Page Numb Header Screenshot v Cystic fibrosis is a hereditary illness causing respiratory issues and recurrent lung infections. It is a recessive disorder (c). Using the details below, fill in the Punnett square to determine probability of an offspring having cystic fibrosis. Mother Father -does not -does not have have cystic cystic fibrosis fibrosis genotype Cc -genotype Cc Mother Father Probability of offspring having cystic fibrosis: ada)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
- Answer the following questions. 1. Construct a map for the genes d,e,f. Assume that: d and e = 3%; e and f = 5%. Give 2 arrangements of the genes/maps. 2. If d and f = 2%, what is the correct arrangement of the genes d,e,f? 3. Consider the fourth gene "g". if g and e = 1.5%, give two possible arrangements. 4. If d and g = 1.5 % give the correct order of the four genes %3DDirection: Identify and explain the etiology of chromosomal abnormality in the given karyotype. KARYOTYPE 1: дек К 6 13 19 7 14 1923 20 1 8 66.25 1559 15 9 21 10 16 22 X 11 17 5 12 042 ANDR 18 YI'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