1. Provide the specific gene involved and the area where the mutation occured in Leigh's syndrome.

Q: 14. Write the karyotype of a Turner syndrome. O A) 2n = 46 - 1 O B) 2n - 1 = 45 O C) 45, X O D) 46 -…

A: Karyotype is defined as the combination of the chromosomes of an individual. It is a laboratory…

Q: 1) Interpret the value of the interference.  2) Map the genes

A: The genes that are located on the same chromosome are considered as linked genes. In this condition…

Q: Options : Sex XY mutations reversal SRY feminization

A: Sex determination is the process that determines the biological sex of an offspring. Humans develop…

Q: Discuss the importance of proteomics in the developmentof treatments for genetic disorders.

A: Omics is the branch of science that deals with the technological approach. This helps to explore the…

Q: 1) What is the prefix that is used when we are expressing 1/1000 of the unit?

A: Units are measured as metric units based on the International System of Units or SI. The units and…

Q: 2. Describe the effect of the mutation that created the Hbs allele on the amino acid sequence of the…

A: A mutation is a change in a DNA sequence. Mutations can result from DNA copying mistakes made during…

Q: The government of Iceland has built a database which contains genetic informaiton about individuals…

A: The genetic material or DNA encodes the information necessary for the functioning of a cell. These…

Q: List and describe the 3 types of fetal testing.

A: we are supposed to answer only first question in case of multiple question posted. Please repost the…

Q: Identify the specific mode of inheritance. 1.) Mae is affected with the disease phenylketonuria…

A: Hi, Thanks For Your Question.  1.) Mae is affected with the disease phenylketonuria (PKU). The PKU…

Q: Chronic Myelogenous Leukemia (CML) -Briefly describe the disease and provide the most common…

A: Leukemia  It is the group of malignant disorder. It affects the blood and blood forming tissues of…

Q: Using PCR to identify whether a patient has an allele of alpha-thalassaemia

A: Genetic testing refers to the tests where abnormalities or mutations are determined or identified in…

Q: 2. Describe the phenotype of individuals whe inherit two copies of the Hbs allele whq Sickle-Cell…

A: * sickle cell Anemia a is blood disorder due to mutation will leads to change in shape of cells into…

Q: People are unable to break down trimethyl-amine, a compound in the diet, resulting in a fish-like…

A: Trimethylamine is a chemical compound that has a pungent odor i.e., smelling like rotting fish,…

Q: 1. The Human Genome Project has demonstrated that in humans of all races and nationalities…

A: The Human Genome Project was an international, collaborative research project whose aim was to map…

Q: 2. Describe the phenotype of individuals who inherit two copies of the Hbs allele Sickle-Cell…

A:

Q: discuss the importance of understanding epigenetics in improving people health

A: Imprinting is an epigenetic procedure that signifies DNA in a sex-dependent behavior and causes the…

Q: ) What are the techniques to verify the extracted genome?

A: Genome extraction is a process by which genitic material is extracted from buccal swab, urine, hair…

Q: Describe the medical applications of human gene therapy in the following diseases: Haemophilia,…

A: Gene therapy is a treatment of a disease where the genetic material is transferred into human cells.…

Q: 9) Describe the steps required to use sequencing DNA to identify your gene of interest after…

A: DNA sequencing is the process of finding the sequence of the nucleotides on a particular short…

Q: 1. Why is it important in Quantitative Analysis to postpone rounding until the calculation is…

A: A quantitative analysis is performed to detect the amount of a specific substance in a sample…

Q: 31.How do your cells turn Genotypes into Phenotypes (be sure to include the explanations of the…

A: I'm this question, we have to answer how cells turns genotype into phenotype.

Q: People are characterized by abnormal red patches, irritated skin, eczema, decreased number of…

A: Genetics is a branch of science that deals in the study of genes, heredity, and genetic variation of…

Q: The majority of direct-to-consumer genetic tests: A) must be obtained through a doctor B) makes…

A: Genetic tests are a type of medical test that looks for changes in genes, chromosomes, or proteins.…

Q: 2. Indicate, using the genetic code, the sequences of amino acids of a part of tyrosinase coded by…

A: Albinism is an inherited genetic disorder that causes the body to produce little or no production…

Q: 1. Do you think the Food and Drug Administration should or should not approve gene therapy…

A: we are answering question 1 only pls repost for rest of question.

Q: A. Enumerate at least 10 genetic diseases and discuss each extensively

A: A genetic disorder or disease is a condition where a gene or a part of gene is mutated or there are…

Q: gene mutation

A:

Q: Compare and contrast preimplantation genetic diagnosis and genetic testing.

A: Pre-implantation genetic diagnosis (PGD) is commonly described as the examination of embryos or…

Q: A disease "D" is caused by a combination of genetic and environmental factors. Polymorphisms in…

A: In the progression of the disease and pathogenesis of disease-causing agents genetic and…

Q: 1. The gene distinguishes retrotransposons from cancer-causing retroviruses. а. gag b. onc С. env d.…

A: Mutations are a sudden heritable change in genome sequence that is responsible for the majority of…

Q: can you help please what is the diagnosis of Chronic granulomatous disease (CGD) and explain the…

A: As we know Bridges-Good syndrome is another or other  name for chronic granulomatous disease (CGD).…

Q: mutations to cause distinct symptoms? (two to three sentences) (Think about why various mutations in…

A: 1 ans.. Muscle dystrophy is a genetic disease, depending on the specific type of MD, the condition…

Q: Decsribe the reason behind the transition mutation that are more common as compared to transversion…

A: DNA polymerase is an essential enzyme for DNA (deoxyribonucleic acid) replication. It works by…

Q: Give the genetic cause (chromosomal abnormality and genes affected), and major characteristics of…

A: Genetic disorders  Disorders that are inherited from parents to their offsprings is know as genetic…

Q: 3. Carol has a sister who has not been tested for the APP mutation. What is the likelihood…

A: Alzheimer's disease is a autosomal dominant disease  that means at least 1 allele  of  mutated gene…

Q: 13 The genetic makeup of an organism is known as the whereas the physical feature of an organism is…

A: Genetics:It is a field of biology which deals mainly with the mechanisms by which traits are passed…

Q: Give the information about DNA mutation types from SNP to large structural variation.

A: Hugo de Vries was the first one to coin the term “mutation.” It is studied under the domain of…

Q: 1. Describe how transgenes can clarify which genecauses a mutant phenotype

A: A transgene is a gene that has been transferred naturally, or by any of a number of genetic…

Q: 10. Which of these is the "gene of interest" a, b, c or d?

A: Gene cloning is a molecular technique of isolating gene or DNA sequence of interest and multiplies…

Q: 6. List two factors that can create incomplete or low quality data in genomics, and 2) their…

A: *Data integration is relevant in genomics because health related decisions depend on it.  * After…

Q: 14. a) What does SVT stand for? b) When should the term SVT be used?

A: The term SVT stands for SupraVentricular Tachycardia. Supraventricular Tachycardia refers to a fast,…

Q: . what is A single gene mutation that affects multiple properties of an organism?

A: Need to find the gene mutation that affects the multiple properties of an organism. There is a…

Q: Give 1 example of syndrome or disorder caused by a mutation then write the cause, type, and effect…

A: Genetic disease caused by mutation includes diseases such as sickle cell anemia, cystic fibrosis,…

Q: Answer the following questions given the pedigree below. Please assume that no other mutations are…

A: The male who is individual number IV 1 is a carrier and has inherited a recessive allele for the…

Q: What is the function of the “junk DNA” in human genome? proper explanation and diagram

A: DNA (Deoxyribonucleic Acid) is the genomic material found in the cells of living organisms that help…

Q: 14. What disorder can be identified in the karyotype? a. Turner's syndrome c. Klinefelter's syndrome…

A: Since you've asked multiple questions, we will answer the first one for you please ask the remaining…