Here is a karyotype made from cancer cells. Which of the following abnormalities can be detected?   A. Translocation   B. Trisomy   C. Monosomy   D. All of the above

Q: Number of chromosomes in the individual's body cells Cell division error that resulted in trisomy 18…

A: INTRODUCTION A karyotype is a collection of a species' or an individual organism's full set of…

Q: what is the likelihood that a male will inherit a sex-linked mutation on the X chromosome from his…

A: Chromosomes are the thread-like structures situated inside the nucleus of the cell. They are made up…

Q: a. The Y axis is the strength of association between prostate cancer and the variant. b. The spike…

A: Genome-wide association studies are used to identify genetic variations in genes associated with a…

Q: Why are individuals with an extra chromosome 21, that causes Down syndrome, more numerous than…

A: Extra Copy of chromosome cause different effects depend upon chromosome number . Some of the extra…

Q: Which of the following does not have an environmental factor thataffects the distribution of the…

A: Phenotype is the appearance and functional properties of the organisms as controlled by genes.

Q: Which of the following does not describe the pedigree analysis ofan autosomal dominant disorder?a.…

A: The DNA (deoxyribonucleic acid) is the hereditary unit of an organism. It consists of purines and…

Q: For the pedigree shown here, the disorder is caused by a recessive (g) autosomal allele. Label each…

A: A tree made of lines and symbols representing the genetic history of person's family is known as a…

Q: If a genetic disease is inherited as an autosomal recessive, one would expect to find which of the…

A:

Q: 10. Examine the pedigree from a family with a genetic disease and answer the questions below: 1:1…

A: Pedigree analysis is a graph that depicts a family tree and shows which family members are…

Q: Which type of chromosome mutation is the following? (><BCDEFG

A: Mutation is any change in the DNA sequence. Any change in the chromosome number is classified as…

Q: Explain how an individual can have Down's Syndrome, and a karyotype that reveals 46 chromosomes.…

A: A genetic disorder is a condition that is caused in whole or in part by a deviation from the…

Q: 1. Fur color of rats is determined by the pathway below. The mating between brown rats of identical…

A: Genotype can be defined as the collection of all the genes present in the body. It is consists of…

Q: A family is tested for spinal muscular atrophy, an autosomal recessive disease, using RFLP. The…

A: Given:  Spinal muscular atrophy -  an autosomal recessive disease (aa) Carrier for spinal muscular…

Q: a. What is the genotype of the mother? b. What is the genotype of the father? c. What are the…

A: Pedigree is a family chart showing the inheritance of a particular trait through several generations…

Q: Name the genetic disorder for individuals A and B. b) Give three characteristics of individual B. c)…

A: A genetic disorder is a disease caused by one or more changes in the DNA sequence which leads to…

Q: Trait W is found in the individuals represented by the shaded symbols in the following pedigree.…

A: Pedigrees are used to investigate the pattern of inheritance of a particular trait through…

Q: When analyzing a normal human male karyotype, all of the chromosomes can be sorted into homologous…

A: Genetics is a study of genes, heredity, and genetic variation in an organism. Living organisms…

Q: Which of the following CANNOT be true about the inheriteance the trait depicted in the pedigree…

A: Inheritance is the process of transmitting the traits from parent to offspring. Traits of an…

Q: A patient has mental deficiency, a short stature, and the mongolian type of the eyelid fold. The…

A: A pateint has mental deficiency, a short stature, and Mongolian type of the eyelid fold. The…

Q: Genes G and H are located on chromosome 18. A woman with the genotype Gg Hh has a child with a man…

A: Nondisjunction refers to the failure of homologous and sister chromatids to divide.

Q: The pedigree below shows the inheritance of a disease that is caused by a late onset, dominant,…

A: Late onset meaning pathological conditions whose signs and symptoms manifest late in the life of an…

Q: Karyotypes can be used to: Map an individual's chromosomes Il. Determine genetic mutations Ill.…

A: Karyotype is  process in which the chromosome of an individual is paired and kept in orderly…

Q: Which of the following statements is/are true of the variegated eye color phenotype in Figure…

A: Introduction :- A phenotype is a set of observable characteristics about a person, such as height,…

Q: The pedigree below shows the inheritance pattern of an autosomal dominant trait in a family. Given…

A: a) I-1, II-4. II-6

Q: In humans, hemophilia is an X-linked recessive condition characterized by the inability of blood to…

A: Genotype is the genetic constitution of an organism for any character and the phenotype is the…

Q: Match each of the following conditions with the correct choice(s) provided on the right. Some…

A: Genes are the functional segments of DNA that code for specific proteins and chromosomes are the…

Q: Trait W is found in the individuals represented by the shaded symbols in the following pedigree.…

A: Pedigree chart shows the inheritance pattern of a particular diseased trait in a family. The chart…

Q: no need to explain just need n=to know if it a.b.c and d. 1.) In a species of dog, a mutant gene…

A: Note: Since you have asked multiple questions, we will solve the first question for you. If you want…

Q: Species I has 2n = 16 chromosomes. How many chromosomes will be found per cell in each of the…

A: According to bartleby guidelines, first three subparts have been answered. Kindly post the remaining…

Q: Given the following frequency, what is the sequence of the chromosome map? D-A: 6%; D-E: 12%; V-E:…

A: A chromosome is a compact structure of a DNA molecule wrapped around some proteins. It is generally…

Q: Hemophilia in humans is due to an X-chromosome mutation. What will be the result of mating a…

A: Introduction  Hemophilia is a genetic disorder that affects the blood's ability to clot normally.…

Q: Autosomal homologous chromosomes   a. are joined at the centromere b. are the same size but…

A: Autosomal chromosomes  These are any chromosomes but not sex chromosomes. They contain gene for body…

Q: A young man went to the doctor because he had small testes and enlarged breasts. Through chromosomal…

A: Chromosomal abnormalities occur due to the duplication or deletion of the section or whole of the…

Q: 5) Crossing over or recombination occurs in _____________which allows for diversity, so that…

A: a. Mitosis is a process of asexual reproduction in which the cells divide into two forming an equal…

Q: An individual has 2n = 14 chromosomes. How many chromosomes do we find in: a. A monosomic b. A…

A: Aneuploidy - It is a chromosomal condition in which there is a gain or loss of chromosome. There are…

Q: During the observation of a baby the diagnosis of Down's syndrome was made. What is the main cause…

A: Normally a baby is born with 46 chromosomes.  But in case of down syndrome babies have extra…

Q: Autosomal nondisjunction can result in

A: Answer: Non-disjunction : It is the error in chromosome number that occurs from the failure in…

Q: B4. In a woman with translocation of a small chromosomal segment from the chromosome 5 on chromosome…

A: MUTATION: Mutation refers to any change or alteration that occurs in the DNA sequence of an…

Q: What is Patient C's karyotype? A. Last song syndrome B. Trisomy 21 C. Marfan syndrome D. Patau…

A: A karyotype is a collection of a species' or an individual organism's full set of metaphase…

Q: Which of the ff. Statement is not true: a. Euploid is a good set of chromosome number b.…

A: Genetic disorders can be outlined as the clinical conditions which occur in the body of an…