Q: Blood Types Person Genotype Blood ty)re Father IAi A+ Child li Mother #1 IAIB AB- Mother #2 IAi B+ A…
A: The presence or absence of antibodies and hereditary antigenic compounds on the surface of red blood…
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: what is the diagnosis of Chronic granulomatous disease (CGD) and explain the genetic mechanism…
A: Bridges-Good syndrome is another name for chronic granulomatous disease (CGD). The distinctive…
Q: Describe an individual with the karyotype shown
A: A karyotype is defined as a collection of an individual’s chromosomes. It is also defined as an…
Q: Explain why a woman carrying the gene forhemophilia can produce two hemophiliac sonswhen she is…
A: A disorder in which blood doesn't clot normally because of a lack of sufficient blood-clotting…
Q: What is the genotype for individual 9? A. X(H) X(h) B. X(h) X(h) C.X(H) X(H)
A: A phenotype is a set of observable characteristics about a person, like height, eye colour, and…
Q: This is an example of Orthologous genes. Ancestral globin gene mes Gu A
A: Orthologous genes are those genes which are found in different species but have similar function…
Q: A type B individual may have the genotype___________ or the genotype ___________.
A: A blood test is used to determine whether the A and/or B characteristics are present in a blood…
Q: Marfan syndrome is inherited in an autosomaldominant pattern. Which of the following is true?a.…
A: Marfan syndrome refers to a genetic disorder of the connective tissue. The extent to which the…
Q: Write the name of lysosomal storage disorders.
A: Lysosomal storage disorder are also known as sphingolipidoses, in which sphingolipids are…
Q: Peter is a 28-year-old man whose father died of Huntington’s disease. Peter’s mother shows no signs…
A: The defect in the gene results in various disorders and this genetic disorder can be inherited from…
Q: In a particular family, children of a diseased mother are all affected, and their maternal…
A: Defective genes cause such mutations or disorders that run down the family and members. Such…
Q: A couple comes to a genetic councilor concerned about their chances of having a baby with cystic…
A: Cystic fibrosis is a progressive, genetic disease that impairs the lungs and digestive system. It is…
Q: Mode of Inheritance: Phenotype (Normal, Affected, or Carrier) Individual Genotype Sex 1-1 1-2 II -1…
A: Pedigree Chart: A pedigree chart is a diagramatic representation that depicts the incidence and…
Q: milar pedigree. One of their daughters is colorblind. Give the genotypes of this nd paternal…
A: Colourbrindness is common hereditary disease. These diseases passed from parents. Mostly…
Q: They are related in str They have identical ba C) they are the result of a
A: Proteins are composed of amino acids, which are bound together by peptide linkage. Amino acids…
Q: An example of a rare genetic disorder in which a person lacks enough blood-clotting proteins caused…
A: These all are genetic diseases . 1 Baldness : Excessive hair loss from the scalp. Hereditary hair…
Q: In references to the "alpha-globin gene locus" or "beta-globin gene locus", the term "locus" means
A: Chromosomes are condensed form of chromatin. Chromosomes consist of two chromatids which are held…
Q: sickle čéll åttacks only normal hemoglobin. Homozygous sickle cell individuals (g sickle cell…
A: Hbn Hbn =homozygous normalHbs Hbs = homozygous recessive with diseaseHbn Hbs= heterozygous normal
Q: Describe the phenotype of individuals who inherit two copies of the Hbs allele Sickle-Cell Disease.
A: Sickle cell anemia (SCA) or sickle cell disease (SCD) is a genetic disorder that occurs due to a…
Q: Which of the following can be identified by anabnormal karyotype?a. Sickle cell diseaseb. Cystic…
A: Cytogenetics is a field of study that focuses on the chromosomes and associated disorders caused by…
Q: Which one of the following disease is Inheritable? A. LeukaemiaB. Colour blindnessC.…
A: The transmission of sex traits from parents to offsprings is called sex-linked inheritance. In…
Q: Sickle cell anemia is an inheritable red blood cell disorder that results in sickle-shaped red blood…
A: HbA encodes normal phenotype. This allele is dominant over HbS allele.
Q: Mrs. Moon has type B blood. Mr. Lee has type O blood. Their son Haneul has type O blood. Make a…
A: There are 4 types of blood groups: A B AB O
Q: 2 II 5 10 Probable pattern of inheritance: %3D
A: The genetic diseases are inherited from family. It could be x- linked or it could be autosomal.…
Q: Ultraviolet light causes thymine dimers to form in DNA. Some individuals are genetically incapable…
A: Genetic variation is very important for evolution, but genetic stability is crucial for survival…
Q: Explain the nondisjunction event that would cause a Turneror Klinefelter syndrome individual.
A: Nondisjunction refers to the failure of homologus chromosomes or sister chromatid to separate during…
Q: Fragile X syndrome What is the prevalence of the trait or disorder? two paragraphs
A: Fragile X syndrome (FXS) is a problem which causes primarily mental and scholarly incapacity. FXS…
Q: PUNNETT SQUARE: GENOTYPES: BB Bb - bb – PHENOTYPES: Belted -: Non-belted-;
A: A Punnett square is used to understand a typical monohybrid and dihybrid cross conducted by the…
Q: Why is DNA testing used for a patient with sickle cell anemia
A: Sickle cell anemia follow autosomal recessive inheritance.
Q: If an individual has type A blood as their phenotype, which genotype(s) could they have? (Mark all…
A: On the basis of antigens located on the surface of red blood cells several dozen of blood groups…
Q: - Trp G CCU Pro CAU - His CGU - Arg U CUU Leu CUC Leu CCC Pro CAC- His CGC - Arg C CUA- Leu CCA Pro…
A: A mutation occurs when the nucleotide sequence of an organism, virus, or extra - chromosomal DNA is…
Q: What happens if a karyotype test is not normal?
A: Karyotype is a chromosome complement of a cell which provides chromosomal aspects such as number,…
Q: Explain why it would be helpful to know if one is carryinga gene associated with a disease.
A: The simplest physical and physiological component of inheritance is the gene. DNA is made of the…
Q: Cystic fibrosis (CF) is the results of DNA changes on chromosome 7. Summarise (3 or 4 sentences) the…
A: Cystic fibrosis is a disease that damages lungs and digestive system. Cystic fibrosis is caused by…
Q: Fill in the blank: Persons with ABO blood type _______________________ are sometimes called…
A: ABO blood type in humans is regulated by three alleles which in turn determine the type of the…
Q: cording to figure 1, what amino acid is found in this part of the beta-globin protein in…
A: Hemoglobin is found in the red blood cell. It is essential for transporting the gases across the…
Q: A man with group A blood marries a woman with group B blood. Their child has group O blood. What is…
A: Blood type in humans is broadly classified into four categories A, B, O, and AB depending on the…
Q: My Diagnosis for Pati Sex: Chromosomal Disorder Justification:
A: Chromosomes are the parts of your cells that contain your genes. Genes are parts of DNA passed down…
Q: Considering the genetics of Lesch–Nyhan syndrome, explain how a female could inherit the disease…
A: Lesch-Nyhan syndrome is a genetic disorder that was categorized by neurological and behavioral…
Q: What is the mode of inheritance for this genetic disease?
A: Pedigree analysis is done to see the inheritance pattern in a family and to determine the…
Q: hY = male, hemophilic %3D a) Show the cross of a man who has hemophilia with a woman who is a…
A: Since you have asked multiple questions, we will solve the first question for you. If you want any…
Q: detacched earlobe phenotype and genotypes
A: A genotype is the genetic makeup of an organism. Phenotype is the observable morphological…
Q: What is Patient B's karyotype? A. Klinefelter syndrome B. Trisomy 13 syndrome C. Down syndrome…
A: Introduction : Karyotype : Karyotype is a representation of complete set of metaphasic chromosome…
Q: Name and describe a test which would show that haemoglobin is a protein.
A: Protein is the basic component of living cells and is made of carbon, hydrogen, oxygen, nitrogen,…
Q: Define these pairs of terms, and distinguish between them. Patau syndrome/Edwards syndrome
A: Some chromosomal disorders are caused due to change in the number of chromosomes in the offspring.…
Q: Identify one human trait, other than skin tone, eye color and stature, that you think has a clinal…
A: Those traits which are genetically inherited often have a clinal distribution. In these traits…
Q: Parents = B+ and AB- Given these are b.g. of parents. If they have a child, what blood types…
A: To determine the blood group of the upcoming generation Karl Landstiener came up with the ABO blood…
Q: The genetically inherited disease shown in the picture above is:
A: this is comes from genetics
is lysosomal storage disease linked to ethnicity of human
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- what is the diagnosis of Chronic granulomatous disease (CGD) and explain the genetic mechanism involved. *do not plagiarized*Altered gene function, on hemophilia AWHAT ACTIVITIES OF DAILY LIVING WILL A PATIENT WITH BROWN SEQUARD SYNDROME (LESION AT C7 RIGHT SIDE) HAVE DIFFICULTY DOING, PRODUCE AN EXPLANATION.
- What is the mode of inheritance for this genetic disease?Treatment of Sickle cell anemia using gene therapy? Please answer at your own words.Considering the genetics of Lesch–Nyhan syndrome, explain how a female could inherit the disease considering that afflicted male patients do not have offspring.
- Write a brief report about down syndrome detailing the signs and symptoms, number of chromosomes, occurrence rate, and prognosisis the suspension of broken cells: None Homogente Pellet Supernatant7849/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.