You possess two alleles for each of your genes. (One from the paternal side and one from the maternal side in each homologous pair of chromosomes.) In simple inheritance,having at least one dominant allele (form of the gene) means you will display the dominant phenotype, and the only way to display the recessive phenotype is to have tworecessive alleles. For example, individuals with the genotypes RR and Rr can roll their tongue (into a U shape). If you cannot roll your tongue, then you know with certaintly youhave the genotype rr. If you can roll your, you would write your genotype as R- (R followed by a dash since you might not know if you are RR or Rr, but either way, you display thedominant phenotype because the first letter is capital.)Match the following traits with their proper genotype using the letters provided in the lab handout.left arm on top when crossing armsblue eyesno middigital hairwidow's peak

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Answered: You possess two alleles for each of…

Human Anatomy & Physiology (11th Edition)

11th Edition

ISBN:9780134580999

Author:Elaine N. Marieb, Katja N. Hoehn

Publisher:Elaine N. Marieb, Katja N. Hoehn

Chapter1: The Human Body: An Orientation

Section: Chapter Questions

Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...

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Albinism, lack of pigmentation in humans, results from an autosomal recessive gene designated a. Two parents with normal pigmentation have an albino child. What is the probability that their next child will be albino? What is the probability that the next child will be an albino girl? If the child is normal, what is the probability that it will be a carrier (heterozygous) for the albino gene?
Armin and Annie are going to have a baby. Annie has dimples in her cheeks (a dominant trait), while Armin does not. You know that Annie's father has dimples in both cheeks, while her mother does not. Her mother must have the recessive trait. Annie's father has the dominant trait, but you don’t know if he is a homozygote or heterozygote. But you still know what Annie’s genotype must be because Annie must have a recessive allele since that is all she could have inherited from her mother. Since Annie has a dimples you know she inherited a dominant allele from her father. What are the chances Armin and Annie’s baby will have dimples? Determine the Phenotype and Genotype and its probability.
a) Which of the four modes of inheritance are consistent with the disease shown in this human pedigrees below? (List the compatible mode or modes) Give an answer for a, b and c b) If the parents in pedigree c have 2 other children, what is the probability that they will carry the disease?
Clark Kent and Lois Lane Kent are about to have a (Super) baby. As Superman, Clark possesses amazing traits, including heat-ray vision. Assume that this is: a) a dominant trait, and b) carried on the X chromosome. If Clark and Lois have a boy or a girl, what is the probability that they will possess their father's amazing abilities? (Remember: females have XX chromosomes, while males have XY chromosomes. The Y chromosome doesn’t carry any of the genes on the X chromosome). X H = Superman’s heat-ray vision allele on his X chromosome Y = Superman’s Y chromosome X h = Lois’s normal vision allele on her X chromosome
In humans, the gene for albinism (a) is recessive to the gene for normal skin pigmentation (A). If two heterozygous persons have children, what is the probability they will have a child who is an albino? What is the probability they will have a child that is a carrier of the recessive gene?
In humans, albinism (lack of skin pigment) is an autosomal recessive trait. The first child of two normally pigmented parents is an albino. Which of the following is true about this family? SELECT ALL THAT ARE CORRECT. A) Their first child (described above) has a homozygous recessive genotype B) The next child born to this couple has a 25% chance of being albino. C) If the next child born to this couple is male, he has a greater chance of being albino. D) The parents are both heterozygous for albinism. E) The probability of their second child being albino is 0% F) If the second and third child born to this couple are albino, the fourth child has 100% chance of also being albino.
Lauren has chronic bronchitis and frequently ends up hospitalized with pneumonia. She has no family history of cystic fibrosis, a serious recessive genetic disorder which affects respiratory and digestive tracts. She and her husband Nat have one child after undergoing fertility treatments to overcome Nat's infertility. They are surprised when their child is diagnosed with cystic fibrosis and the genetic counselor tells them that they each also have the condition, which causes their bronchitis and infertility. Which of the following would be a reasonable explanation of their situation? Although the underlying disease is genetic, the severity of the disorder if influenced by environmental variation. Cystic fibrosis displays variable expressivity. There are different alleles of cystic fibrosis which cause differing forms of the disease. There are different alleles of cystic fibrosis which cause differing forms of the disease and Cystic fibrosis displays variable expressivity are the only…
Can you please not type the answer can you write it on a paper
Adenike and her partner, Debare, are expecting their first child. Adenike is healthy as are her two sisters but her brother has PKU, a recessive disorder of the PAH gene. Genotypically he must be pah-/pah-. Neither of Adenike's parents has PKU but both of her grandmothers did. Debare is a carrier of Sickle Cell trait, which means he has one allele for wildtype hemoglobin (HbA) and one allele for Sickle Cell (HbS), making him HgA/HbS. More importantly, he has two alleles for Marfan Syndrome, a pleiotropic dominant disorder that can affect up to 30 different traits (M+/M+). No one in Debare's family has ever had PKU and no one in Adenike’s family has ever had Sickle Cell or Marfan Syndrome. They consult a genetics counselor over concern of the health of their baby. The genetics counselor collects the medical histories of three generations; their grandparents, their parents, and them. In her calculations, she produces a phenotypic key that indicates M = Marfan, Hb = sickle cell, and pah-…
In humans, blue eyes are inherited as a recessive autosomal trait and color blindness is an X-linked recessive trait. A woman with blue eyes and normal color vision (her father was colorblind) marries a man who has normal color vision. The man has brown eyes, but his mother had blue eyes. What is the probability that this couple will have a child with normal vision and blue eyes?
Amanda Sefton (Daytripper) has normal fingers and toes and normal color vision. Her mother is normal in all respects, but her father is color blind (X- linked recessive) and syndactylous (autosomal dominant). Kurt Wagner (Nightcrawler) is color blind and syndictylous. His mother has normal color vision and normal fingers and toes, but he didn't know his father. As their genetic counselor, answer the following questions based on Kurt and Amanda marrying and starting a family. What is the probability of having a child that has syndactyly? (Enter your answer as a decimal; Example = 0.8782)
Genetic Inheritance Patterms Retinitis pigmentosa (RP) can be autosomal recessive, autosomal dominant, or x-linked. Apparently the dominant forms are often less severe. Eric's form of RP is Usher's Syndrome, which is an autosomal recessive inheritance (i.e., you must get a copy of the defective gene from your Mom and one from your Dad). Autosomal means it is not carried on one of the chromosomes that determines sex. Usher's Type II is recessive, so for Eric this means that both his Mom and Dad are carriers of this condition. His brother, Dirk, does not have any symptoms of RP. Draw a pedigree of Eric's family showing possible genotypes and chances of having RP. Your pedigree must include his parents, Eric, his brother Dirk, and a potential daughter of Eric's. Draws a pedigree that shows the correct genotypes and chances of having retinitis pigmentosa for Eric and his family. D.Focus (United States) a S W 37 F 八口

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