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 the phenotype of individuals who inherit two copies of the HbS allele-Sickle Cell Disease.
A: Sickle cell anemia It is a genetic disorder that affects erythrocytes(RBC) causing them to become…
Q: Which of the following was used to label protein in the hereditary material for genetic information…
A: Hershey and Chase inserted the radioactive elements in bacteriophage by adding the isotopes in their…
Q: Does this statement is a example of a phenocopy? Explain your reasoning. Q. Phenylketonuria results…
A: Phenylketonuria is a genetic disorder characterized by the deficiency or absence of the enzyme…
Q: Using the blood types listed, indicate the possible gene pairs. Make your own table and write your…
A: RBCs of the blood have surface antigens. These surface antigens are inherited trait. Depending on…
Q: Differentiate between D-value and z-value.
A: Introduction Sterilization is the process of completely eliminating or destroying all microbial…
Q: discuss briefly the results of Gregor Mendel's experiment on the colors of the pod of pisum sativum.
A: NOTE: please note that as per our company's honor code, citing external refernces are not allowed.…
Q: The region of a chromosome that encodes a single protein is called a _________, each of which can…
A: Genes are present in the chromosomes they are segments of (DNA or RNA) Deoxy ribo or ribonucleic…
Q: Please write your complete solution (paper). Albinism in humans is inherited as a simple recessive…
A: Genes store genetic information in the form of DNA, which may be converted into functional proteins…
Q: please answer the question provided in the picture about the black allele gene asap please
A: INTRODUCTION Translation is the process of translating the sequence of a messenger RNA (mRNA)…
Q: In Figure 5-32, what do the half-red, half-blue segments represent?
A: the half-red, half-blue segments represent:
Q: HH alleles are ________________ genotype.
A: Genes are the specific codes of these amino acids which produces a protein and alleles is the…
Q: The profile includes 4 STR loci. (D8S1179, D21S11, D7S820, CSF1PO) At how many of these is the…
A: Short Tandem Repeat Analysis STR analysis is a molecular technique by which short tandem repeats…
Q: Define mutant allele
A: The genome of an organism consists of the genetic information that is inherited by its offsprings.…
Q: Explain the following term: Allele:
A: DNA is the genetic material present in most of the living organisms. The DNA is made up of 4…
Q: Alpha thalassemia is a hereditary blood condition that results in varying levels of anemia. It is…
A: Hemoglobin is an oxygen carrier protein that is made of four chains, two alpha, and two beta chains.…
Q: Define ‘gene’. What is an allele and loss-of-function alleles? What do these alleles tell us about…
A: "a DNA phase that contributes to the phenotype/characteristic of an organism."
Q: Animation 12.1: This table shows results from allele specific oligonucleotide hybridization analyses…
A: Blotting techniques are the methods used in the molecular biology for the identification or…
Q: Match these genetic terms to their descriptions
A: Monomer are combined to form polymer through dehydration reaction.
Q: Your classmate claims that they can correctly identify the genotype of her guinea pig just by…
A: Genotype is the stored information in the genome or DNA of the organism.
Q: Explain the following diagram. It refers to a pedigree on the disease called phenylketonuria.…
A: The pedigree analysis describes the process of interpretation of information displayed as a family…
Q: Alternate form of the same genes are called
A: The body cells contain pairs of homologous chromosomes. The two chromosomes of each pair have the…
Q: What is the labeled part of these figures?
A: Answer: SHOOT and ROOT system are the two parts of a plant where shoot includes the upper portion…
Q: a. For the E.coli haploid genotype below, determine the phenotype for the following proteins. Assume…
A: The lactose operon is an example of inducable operon in which the expression (or transcription) of…
Q: Paste or draw a picture of a Punnett square showing a cross between an individual with the disorder…
A: Sickle cell anaemia is an autosomal recessive trait. Let HbA encodes normal phenotype and it is…
Q: A RFLP is discovered that is linked to the gene for Duchenne’s muscular dystrophy (DMD). DMD is an…
A: RFLP (Restriction Fragment length polymorphism) : RFLP (Restriction Fragment length polymorphism is…
Q: in the following pedigree, how close in genetic distance (cM) is SSLP-g86 to thể disease allele?…
A: A pedigree chart of family usually depicts the traits of linkage or recombination that descends down…
Q: a. For the E.coli haploid genotype below, determine the phenotype for the following proteins. Assume…
A: Lac operon Lac operon or the lactose operon is a gene expression system in E Coli. and many similar…
Q: Select and order the images representing 1. the alleles that code for sickle cell anemia 2. the…
A: Sickle cell anemia (SCA) is caused by a mutation in the gene that codes for the beta-globin…
Q: Please write your complete solution (paper). Albinism in humans is inherited as a simple recessive…
A: Alleles at the alternative forms of a gene that are located on the same locus of a homologous…
Q: When a phenotype varies continuously withlevels of protein function, why incomplete dominance…
A: Genotype controls phenotype and it is because gene directs the protein production, protein, in turn,…
Q: >chromosomal…
A: Codons are trinucleotide sequence that codes for specific amino acids and there are totals of 64…
Q: Il-- Results from a single locus probe DNA fingerprint analysis for a man and woman and their four…
A: Introduction DNA fingerprinting is a critical technology that assists investigators in establishing…
Q: Explain the following diagram. It refers to a pedigree on the disease called phenylketonuria.…
A: Phenylketonuria is an inherited disorder that increases the levels of a substance called…
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: Give the genetype t phenstype of the offspring,
A: Method:- The method done with the pencil is not the most accurate way to draw a Punnet Square.…
Q: Draw each of the following base pairs: A-T, G-C, and U-
A: Adenine, guanine, cytosine and thymine are the nitrogenous bases which are present in DNA and in RNA…
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: Examine the following karyotypes and answer the questions about each karyotype in the table below.…
A: Chromosomal abnormalities can occur due to non-disjunction i.e. a pair of chromosomes fails to…
Q: For gain-of-function disorders, which of the following treatment strategies is the be . A. Gene…
A: Introduction :- Gain-of-function (gof) genetic illnesses are caused by the ectopic or enhanced…
Q: Both recombination and random fertilization are important for what major biological process? Be…
A: Introduction In Genetics, Recombination Is The Fundamental Process For Introducing Variation Into…
Q: What are two possible explanations for why the same genotype (DNA) can result in different…
A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…
Q: create picture of a Punnett square showing a cross between an individual with the disorder and a…
A: Sickle cell anaemia is an autosomal recessive trait. The HbA allele encodes normal phenotype. It is…
Q: If you have a dihybrid organism with genotype AaBb whose alleles are in repulsion (trans)…
A: Trans configuration meaning: In genetics,two types of configurations are found-cis and trans Trans…
Q: Would you be able to draw a circular map of the seven genes? I have trouble with correct position of…
A: The DNA replicates itself several times during the replication process. It is a biological…
Q: If two unaffected parents have an affected child, they must be what of the gene
A: Given condition: Two unaffected parents have an affected child. This is possible only when both…
Q: The A and B alleles code for different forms of the enzyme ___(two words) that recognize different…
A: Chemicals are proteins that go about as organic impetuses (biocatalysts). Impetuses speed up…
Q: What is difference between normal primer and degenerative primer
A: Primer: These should be 18–24 nucleotides in the length and it provides for the practical annealing…
Q: Answer the following questions given the pedigree below. Please assume that no other mutations are…
A: Pedigree is a family chart showing the inheritance of a particular trait through Several generations…
Q: Match each formatting of "white" to what it represents in genetics. options: white WHITE…
A: Question - Match each formatting of "white" to what it represents in genetics. options:…
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- A 30 - year - old woman was undergoing therapy for b-thalassemia,a recessive trait caused by absence of or reduced synthesis ofthe hemoglobin b chain, a subunit of the oxygen-carrying moleculein red blood cells. In this condition, red blood cells are rapidlydestroyed, freeing a large amount of iron, which is deposited in tissuesand organs. The blood transfusions the patient had received every twoor three weeks since the age of 7 to stave off anemia were furtheraggravating iron buildup. Her major organs were showing damage, andshe was in danger of death from cardiac disease. Her physician suggestedthat she consider undergoing a hematopoietic (bone marrow)stem cell transplant (HSCT). Since these stem cells give rise to redblood cells, such a transplant could potentially restore her health. Whilethis might seem like an easy decision, it is not. Advanced cases havea high risk (almost 30 percent) for transplantation-related death. At thispoint, the woman is faced with a difficult and…Genotypes and Phenotypes I have gap teeth, but my husband doesn't. How do I explain how my children got gap teeth just like me, using Genotypes and PhenotypesAnalysis of X-Linked Dominant and Recessive Traits Suppose a couple, both phenotypically normal, have two children: one unaffected daughter and one son affected with a genetic disorder. The phenotype ratio is 1:1, making it difficult to determine whether the trait is autosomal or X-linked. With your knowledge of genetics, what are the genotypes of the parents and children in the autosomal case? In the X-linked case?
- Genetics in Practice case studies are critical-thinking exercises that allow you to apply your new knowledge of human genetics to real-life problems. Case study Michelle was a 42-year-old woman who had declined counselling and amniocentesis at 16 weeks of pregnancy but was referred for genetic counseling after an abnormal ultrasound at 20 weeks of gestation. After the ultrasound, a number of findings suggested a possible chromosome abnormality in the fetus. The ultrasound showed swelling under the skin at the back of the fetuss neck; shortness of the femur, humerus, and ear length; and underdevelopment of the middle section of the fifth finger. Michelles physician performed an amniocentesis and referred her to the genetics program. Michelle and her husband did not want genetic counseling before receiving the results of the cytogenetic analysis. This was Michelles third pregnancy; she and her husband, Mike, had a 6-year-old daughter and a 3-year-old son. At their next session, the counselor informed the couple that the results revealed trisomy 21, explored their understanding of Down syndrome, and elicited their experiences with people with disabilities. She also reviewed the clinical concerns revealed by the ultrasound and associated anomalies (mild to severe intellectual disability, cardiac defects, and kidney problems). The options available to the couple were outlined. They were provided with a booklet written for parents making choices after the prenatal diagnosis of Down syndrome. After a week of careful deliberation with their family, friends, and clergy, they elected to terminate the pregnancy. Do you think that this couple had the right to terminate the pregnancy in light of the prenatal diagnosis? If not, under what circumstance would a couple have this right? What other options were available to the couple?Variations in Phenotype Expression A genetic disorder characterized by falling asleep in genetics lectures is known to be 20% penetrant. All 90 students in a genetics class are homozygous for this gene. Theoretically, how many of the 90 students will fall asleep during the next lecture?Don't copy from Google or any other platform!! Thanks Once a genetic disorder in an adult is treated successfully through gene therapy, it is highly unlikely that the person's children will inherit the gene(s) for the disease. a. True b. False
- Trait: NeurofibromatosisThe dominant form is neurofibromatosis, caused by the production of an abnormal form of the protein neurofibromin. Affected individuals show spots of abnormal skin pigmentation and non-cancerous tumors that can interfere with the nervous system and cause blindness. Some tumors can convert to a cancerous form.The recessive form is a normal protein - in other words, no neurofibromatosis. Situation:Karina wants to know from whom she got her disorder. Her grandmother Ana has neurofibromatosis. Ana marries Angelo, who does not have the disease. They both have children named Christine (eldest), Monica, Joseph, Marco, and Yna (youngest). Monica, Marco, and Yna have the disorder out of the five children. Christine marries a man with the disorder, and they have two daughters, Kadita and Karina, who both have the disorder, and another daughter, Karrie, who does not have neurofibromatosis. Yna, on the other hand, marries a man with the disorder. They have four children,…Fill the blank A DNA _________ contains allele-specific oligonucleotides(ASOs) for millions of SNP loci. Under the properconditions, a probe made of fluorescently-labeledgenomic DNA fragments binds only to complementaryASOs, allowing these loci to be genotyped.Clinical or phenotypic heterogeneity, in which different mutations in a gene may result in different phenotypesTRUE oR FALSE ASAP NO EXPLANATION NEEDED
- Galton’s traits are readily observed in everyday life. What did Galton discover?Epistatic mteraction means that one gene----------the effect of another gene.(A) Prometic (B) Mask(C) Accelerate(D) None of theseGENETICS Alberta is phenotypically normal, but her brother (Rodrigo) has albinism, which is caused by an autosomal recessive mutation. The probability that Alberta is a carrier is______?