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*WHAT ACTIVITIES OF DAILY LIVING WILL A PATIENT WITH BROWN SEQUARD SYNDROME (LESION AT C7 RIGHT SIDE) HAVE DIFFICULTY DOING, PRODUCE AN EXPLANATION.Altered gene function, on hemophilia A
- What is the mode of inheritance for this genetic disease?Considering the genetics of Lesch–Nyhan syndrome, explain how a female could inherit the disease considering that afflicted male patients do not have offspring.Treatment of Sickle cell anemia using gene therapy? Please answer at your own words.