How can NF1 be spontaneous? Include the following terms: -genotype - phenotype - homozygous - heterozygous - inheritance - alleles - dominant - recessive
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Q: Plsssssssss helppppppppp, how can NF1 be spontaneous? Include the following terms: -genotype -…
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- Plsssssssss helppppppppp, how can NF1 be spontaneous? Include the following terms: -genotype - phenotype - homozygous - heterozygous - inheritance - alleles - dominant - recessivehello, there’s this question I need help on but I don’t want no google help with! I need to learn this It asks If a person who is heterozygous for polydactyly -having 6 fingers instead of 5 an autosomal dominant trait marries a person who is normal what is the probability that they will have four normal children and two children with extra fingers (I want this to be a clear answer without it being way too wordy just straight forward)TTGG ttgg F1 TG tg F2 TtGg Which types of genotypes are represented in F1 and F2 in the above figure, respectively? heterozygous and heterozygous heterozygous and homozygous homozygous and heterozygous homozygous and homozygous
- Let us practice it again! Analyze the pedigree below to answer the questions that follow. Huntington's disease a disorder in which nerve cells waste away, or disintegrate, is passed down through families. certain parts of the brain Huntington's diseate llustration ereated in htps://pregenygenetion.com/ 1. What members of the family above are affected with the Huntington's disease? 2. Tnere are no carriers ior Huntungton's disease you either have it or you do not. Is Huntington's disease caused-by a dominant or recessive trait? 3. Identify the genotypes of the following individuals using the pedigree above. (homozygous dominant, homozygous recessive, heterozygous). I- 1 II -1: II -3: III - 4 : 4. How many children did individuals I-1 and I-2 have? 5. How many girls did II-1 and II-2 have? How many have Huntington's Disease? 6. How are individuals III-2 and II-4 related? I-2 and III-5?A type of red-green colorblindness is inherited recessively on the X chromosome. A woman who is a carrier had children with a male that is not affected by the disease. Show your answers with the use of a Punnett square • What is the probability (% or likelihood) that a child is affected by the disease? • What is the probability (% or likelihood) that a son is a carrier? (Careful!) • Is there a chance that a girl of the couple is affected by the disease?YOUR SISTER DIED FROM TAY-SACHS DISEASE, INHERITED AS A RECESSIVE ALLELE (t). you're married and planning to start your family. you're worried about the disease and decide to have genetic testing to see if you or your spouse is a carrier of the tay-sachs allele. the test results show that you're a carrier of the allele, but your spouse isn't. what is the probability that you and your spouse will have a child with tay-sachs disease? show your work.
- Hemophilia is an X-linked recessive trait. The wife is hemophiliac, but the man has normal blood clotting. What is the probability that their SONS will be hemophiliac? 25% 75% 100% 50% 0%The allele for color-blindness is carried on the X chromosome. Making color blindness (a recessive trait) an X - linked trait. A colorblind make and a carrier female for color blindness. (But is not colorblind herself) have a child. Show your work! A) what is the % chance that their son will be color blind? B) what is the % chance that their daughter will be color blind?Rolly's APPLE ACK Free stu X O Leaming Lab Varsity Tutors + tutors.com/learning-lab/assessment/2eb9c784-88d7-4224-91d8-87c72f8edeb1 r rr rr Which best describes the parent genotypes in the punnet square provided? A Homozygous dominant and heterozygous B Two heterozygous C| Homozygous recessive and homozygous dominant D Homozygous recessive and heterozygous I don't know Next Question
- Hemophilia, disease in which the blood lacks a clotting factor, is caused by an X linked recessive gene. Joe doe not have hemophilia and Lucille is heterozygous for the condition. What is the chance that their MALE child will have hemophilia? (Note: you are calculating the probability for their MALE children only, in other words if they have 1 male child, what is the probability that he will be born with the disease?) 0% 1/4 or 25% 2/4 or 50% 3/4 or 75% 4/4 or 100%A mother who is heterozygous for Huntington’s disease (child from mother in #8) and a father who is homozygous normal want to have a baby. What genotypes and phenotypes are possible for their child?What is nondisjunction? Why does it cause chromosomal abnormalities? What is aneulploidy? Trisomy? Monosomy? Which kind of monosomy always results in miscarriage in early pregnancy? What do these terms mean: genotype, phenotype, allele, homozygous, heterozygous? Be able to recognize single gene inheritance patterns [autosomal dominant, autosomal recessive, X linked recessive] from a pedigree. Also, how are simple Mendelian traits transmitted? What genotype produces the phenotype? Why do some inheritance patterns result in many more males than females showing the phenotype? What inheritance patterns do Huntington disease and sickle cell anemia, and hemophilia follow (autosomal dominant or autosomal recessive, or X-linked recessive)? What are some of the symptoms of these diseases?
