Q: What is the cause of Wolf-Hirschhorn and make sure to explain specifically why the karyotype of your…
A: Wolf-Hirschhorn syndrome (WHS) is a genetic disorder that affects many parts of the body. The major…
Q: describe what is CNVCopy number variant?
A: The human genome consists of 6 billion chemical bases or nucleotides of DNA packed into two sets of…
Q: Illustrate and give the normal sequence and the mutated sequence in Leigh's syndrome
A: A disease is a state of unhealthiness of the physical body, mind and social interaction. A disease…
Q: Explain how it is possible for a person with a translocationor an inversion to be phenotypically…
A: Chromosomes are the condensed packaged structure of the genetic material of an organism. The…
Q: what is the phenotype of the attached images?
A: Genes are the functional unit of heredity. It carries information from one generation to another.…
Q: what is dosage compensation.?
A: Sex of an organism in various species depends on the type and number of sex chromosomes. In species…
Q: What is Prenatal genetic diagnosis ?
A: Prenatal diagnosis involves non-invasive and invasive techniques. The non-invasive technique…
Q: • What is the causative gene mutation in these diseases? • What amino acid and/or protein domain is…
A: this is a multipart question and according to our guidelines we are allowed to answer only 3 parts…
Q: Explain the genes responsible for complex diseases such as coronary artery disease ?
A: “Coronary artery disease (CAD)” is a complex disease that is considered the leading cause of death…
Q: Regarding albinism, with adavances in fields such as gene therapy and stem cell research, is there a…
A: Introduction :- Albinism is an inherited condition in which the rate of melanin production is…
Q: Define deletion-insertion polymorphisms (DIPs)
A: Insertion is a mutation in which one or more nucleotide base pairs are added into a DNA sequence.…
Q: What the grandparents' genotypes are? Why doesn’t the father (II-1) have the disease breast cancer?…
A: Genetic inheritance is the process by which genetic information is passed from the parents to the…
Q: What are the possible genotypes of the PTC locus?
A: * genotype means collection of genes that refers to two alleles of a particular gene and genotype…
Q: Explain an example of single-nucleotide polymorphism (SNP) associated with disease.
A: Answer- Single nucleotide polymorphism is the DNA sequence variation at the single site.
Q: Why Recessive CF disease alleles either produce no CFTR or produce nonfunctional or less functional…
A: Cystic fibrosis (CF) is a classical example of recessive disease. It is a disease that is inherited.
Q: What is the genetic basis of the symptoms of Down syndrome?
A: Ans: In humans various diseases or disorders are caused by chromosomal aberrations or mutation in…
Q: How can Cri-Du-Chat syndrome be diagnose with karyotyping?
A: Karyotyping is a genome-wide snapshot of an individual's chromosomes. It's a collection of a cells…
Q: Why are maternal effect genes so difficult to identify via mutant analysis?
A: Introduction :- In an offspring , the genes are contributed by both of the parents but the mother…
Q: What is an allelic mutation?
A: Gene is a unit of heredity that is transferred from 1 generation to another, from parents to their…
Q: What category of genetic disorders does albinism disord
A: Answer Albinism is a single gene defect and it is a type genetical disorder.
Q: physical appearances of individuals affected by the abnormality structure of deletion, inversion,…
A: The phenotypes of individuals are effected by numerous factors. As much as it depends on factors…
Q: Define the noninvasive prenatal genetic diagnosis (NIPGD) technique ?
A: KEY WORDS :- Prenatal - It is the period before delivery of the baby. When fetus is growing inside…
Q: What is anomic aphasia?
A: The anomia is generally a language disorder - inability to express or communicate. It will slowly…
Q: What is Intron retention type of alternativesplicing ?
A: A portion in mRNA that codes for protein is termed as exon. The non-coding region is termed as…
Q: What cause of the genetic disease
A: (Please note that we are not supposed to provide links to the information.) Genetic disorders are…
Q: Define common variants
A: A common variant is a part of a hypothesis "Common diseases-common variant" that accounts for the…
Q: describe Deletion-insertion polymorphisms (DIPs)
A: Polymorphism: Many forms of a allele is termed as polymorphism. The polymorphism leads to the…
Q: determining coat color is the agouti gene?
A: The coloration, pattern, and length of the cat fur is governed by numerous genes and is determined…
Q: What term is used to describe the dip at the region marked by 4? What is its purpose?
A:
Q: what are the steps for diagnosing Cri-Du-Chat syndrome using Karyotyping?
A: The analysis of cri du chat disorder is affirmed by an through clinical assessment, Identification…
Q: What causes short stature in Turner syndrome?
A: Answer: Introduction: Turner syndrome (TS) is commonly found chromosomal disorders. It appears…
Q: Compare and contrast the molecular and phenotypic features of Prader-Willi and Angelman syndromes.
A: Prader villi and angle man syndrome are imprinting disorders. Both are related to abnormalities in…
Q: What are similarities between Jacob Syndrome and Patau Syndrome?
A: Jacob Syndrome is a chromosomal aberration caused by the non-disjunction of the Y chromosome. They…
Q: Describe the exact DNA mutation that has occured, to create the mutant dystrophin allele.
A: Complex of dystrophin and glycoprotein (DGC). Dystrophin is a rod-shaped protein that binds the…
Q: Hemophilia , Beta Thalassemia , and Sickle Cell Disease what do all of these disorders have in…
A: A mutation is a change in the sequence of the DNA. Mutations can result from the following: DNA…
Q: What is the significance of the Philadelphia chromosome, and how is it related to leukemia?
A: Chromosomes are the structures present in the nucleus that appear thread like and contain genes.…
Q: Over a thousand different alleles at the CFTR locus have been discovered that can cause cystic…
A: Cystic fibrosis (CF) is a genetic illness that makes bodily fluid develop in a patient's lungs.…
Q: What is the Philadelphia chromosome? How is this chromosome related to cancer? Identify how this…
A: A chromosome could be a dna (deoxyribonucleic acid) molecule with some or all of the genetic…
Q: b. How is the inheritance pattern of Jervell and Lange-Nielsen syndrome similar to that of familial…
A: Long QT syndrome is a heart condition in which the heart's electrical system is abnormal. The heart…
Q: What are the treatments for sickle cell anemia disorder and what are the possible treatments…
A: Sickle cell anemia disorder is a type of genetic or inherited blood disorder that results in the…
Q: Indicate how D-value and z-value differ.
A: Introduction A microbe, or microorganism, is a microscopic organism. It may occur as a single-celled…
Q: The karyotypes shown here depict chromosomal abnormalities. Name the syndromes and if they are male…
A: "Genes" are the fundamental unit of heredity. They store genetic information in the form of DNA,…
Q: What the genetic disease talk about? What cause of the genetic disease?
A: Genetic disease means the disease that is caused by a mutation in the genome and these mutations are…
Q: Are changes that cause high FST found equally across the genome? What areas of the genome would be…
A: The fixation index is a measure of the population difference due to the genetic structure. It is the…
Q: How do I construct these punnets squares?
A: Punnet square The Punnett square was first time designed by Reginald C. Punnett. It is use to…
Q: Compare and contrast the molecular mechanisms leading to FX syndrome and to FSHMD.
A: Introduction :- A gene originally known as FMR1 gene by scientists and responsible for FXS is…
what is the diagnosis of Chronic granulomatous disease (CGD) and explain the genetic mechanism involved. *do not plagiarized*
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- State the diagnosis of Chronic granulomatous disease (CGD) and explain the genetic mechanism involved. Briefly explain it and give the sources (links)/references you used.Duchenne muscular dystrophy describe the function of the gene and gene product as well as the phenotype (clinical picture). Explain how mutations in the gene and protein could contribute to the observed phenotype. Discuss the protein structures associated with the condition. How is it helpful in understanding gene’s function and in possible explaining of the pathology.Explain why PID is considered a serious condition.
- Analyze the pathophysiology Crohn’s disease and relate genetic issuesSelect two of the following diseases and discuss cause, predisposing factors and identify if it is considered a Genetic Disease or a Congenital defect: 1) Phenylketonuria 2) Cystic fibrosisHow is the patient affected with usher syndrome? At the:-Organism level-Cellular level-Biochemical/molecular level
- hi, can I please get help on a case study on nueroanatomy I have been struggling for a couple of hours now and can't seem to understand the study to answer the following questions. is there any way or format that i can get help. I would really appreciate it. thanks! 1. Based on the information in the case, what is the most likely neuroanatomic location for a single lesion that can explain all of the patient’s symptoms and signs? In your own words, explain how you arrived at that localization. 2.What are some possibilities for the nature of the lesion (e.g., stroke, tumor, trauma, etc.)? In your own words, explain your rationale for these options. 3. How does the laboratory data and neuroimaging demonstrate the actual lesion for the patient? Describe how you interpret the data in your own words. 4.How was the patient was treated, and how did they subsequently fare? Describe the treatment plan in your own words.a) What does SVT stand for? b) When should the term SVT be used? 14.7849/variants/881590/take/13/ awered Match each description with the associated skin disorder. NO infection of the sebaceous gland caused by a blocked duct blue tint to the skin caused by lack of oxygen overgrowth of adipose tissue in the hypodermis raised bumps on the skin caused by an allergic reaction autoimmune response that destroys melanocytes, causing pale spots on the outbreak of the HSV virus around the mouth or nose ●00 a. d. cyanosis lipoma cold sores e. urticaria f. vitiligo Q 12 ☆ All Changes Jared.