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- Five [GENETICS] Instructions; — Answer the questions properly. — Do not copy in Google or Bartleby. — Plase make sure the answer are correct. Failed to follow the Instructions will report directly to Bartleby. THANK YOU!I need help finding the correct answers. the formula I used is % idenity=(length of the aligned region- the number of mismatches)/length of the aligned regionx100 for sequnce `1 and 3 I got a 70 percent idenity and 3 mismatches I think I am counting the wrong mismatches? can someone correct my answers and show me how they got theres and do not use cheggPatient A's History Patient A is the nearly-full-term fetus of a forty year old female. Chromosomes were obtained from fetal epithelial cells acquired through amniocentesis. Patient A's Karyotype See attached picture 1. Using the correct notation for interpreting karyotypes, give your diagnosis for the conditions of each patient. (standard notation and phenotype (e.g. 47, XY, +21, male Down syndrome)): References
- "preliminary fact gathering stage" trying to find out what baby #3 will look like L = thin lips l - full lips Mrs. Spud Mr. spud Pheno: l Pheno: L Geno: ll Geno: Ll 1st Child 2nd child Pheno: L Pheno: l Geno: Ll Geno: LlThree [GENETICS] Instructions; — Answer the questions properly. — Do not copy in Google or Bartleby. — Plase make sure the answer are correct. Failed to follow the Instructions will report directly to Bartleby. THANK YOU!Patient B's History Patient B is a 28 year old male who is trying to identify a cause for his infertility. Chromosomes were obtained from nucleated cells in the patient's blood. Patient B's Karyotype 1. Using the correct notation for interpreting karyotypes, give your diagnosis for the conditions of each patient what diagnosis would you give patient B? (standard notation and phenotype (e.g. 47, XY, +21, male Down syndrome)) References:
- I need help with the following questions and there are multiple parts and I dont understand! Scientists have recently inserted a gene to create a mouse with an increased capacity for learning and memory- basically increasing the mouse’s IQ. Normal, average human IQ is around 100, above that is considered highly intelligent while an IQ below 70 is considered to indicate mental disability. In the future, if this treatment could be applied to humans, it could increase IQ by 30 points. A couple has a son with Down’s syndrome giving him an IQ of 70. They want to use the therapy to increase his IQ to 100 in order for him to function normally. This is considered to be gene therapy, where technology is used to help a person function better. A second couple has a son with an IQ of 120. They want to use the technology to bring his IQ up to 150. They feel he would have a better chance of getting into a prestigious university. This is called gene enhancement where technology is…Please Answer Correctly with explanation, Don't Copy from internet and nswer all parts EITHER Correct OR Incorrect. 1. Every cell in Clayton's body has the same genome. 2. The genes on homologous chromosomes are in the same order. 3. Anna's nuclear genome is identical to that of her siblings in terms of sequence.Retinoblastoma: The Hits Just Keep Coming Part IV – Time to Reconvene Question Since Julie is indeed a carrier of the mutated RB1 allele and Chris is homozygous for the wild-type allele, what is the likelihood that their next child will inherit Julie’s RB1 mutation? Part V – A Different Kind of Hit Question Chris does not have an RB1 mutation, and is therefore homozygous wild-type. Julie is heterozygous for the mutation. However, Kay has inherited a different RB1 mutation than the one her mother carries. Therefore, Kay did not receive her mother’s mutant allele. Assuming that Chris really is the father, what other explanation might there be for how she got a germline mutation?
- Please help me answer these 3 questions. Thank you so much 2. What syndrome is also called asr criminal syndrome? 3. How many number of autosomes and sex chromosome are there in alagille syndrome? 4. What type of syndrome that has 45 autosomes and sex chromosome, the abnormality is numerical abnormality and sexual aneuploidy and the patient has a low life expectancy? (note: aside from turner's, patau, and down syndrome)Patient F The mother wants to determine whether her unborn child is afflicted with genetic disorder. Amniocentesis was performed and chromosomes from amniotic fluid were obtained for karyotyping. Complete Patient F's Karyotype.14. Dr. Jablonski describes learning that low folate levels are linked to severe birth defects as a “eureka moment.” Explain what she means by this. Can you please help me with this question?.