In this exercise, you will take a look at a patient's karyotype and identify the genetic disorder. Link e Patient Ce is O Trisomy 13 Syndrome O Down's Syndrome Klinefelter's Syndrome O patient's problems are due to something other than an abnormal number of chromosomes.

Q: Draw two replicated, un-condensed, homologous chromosomes that have the genes A and E on them. This…

A: Homologous chromosomes - Homologous chromosomes is the pair of DNA. These chromosomes are present in…

Q: s alternative form of a single gene is known as  parental, dihybrid, reciprocal, allele, or…

A: Alleles are variant forms of a gene. Individuals receive one allele from the father and one from the…

Q: Which of the following is true for linked genes? a) Alleles of linked genes are often inherited…

A: According to Mendel, units of inheritance are discrete, occurs in pairs i.e. alleles and can stay in…

Q: atient D died shortly after birth, with a multitude of anomalies, including microcephaly, low set…

A: A gene is a unit of hereditary present in thousands of numbers on the helical strands of…

Q: Cystic fibrosis is a genetic disorder that damages the tissues of the lungs. A – normal a -…

A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…

Q: our blood type is a: A. genotype B. phenotype

A: Blood group depends upon the presence of surface antigen present on RBC. These antigen are encoded…

Q: In an epic battle, the Green Goblin was able to wound Spider-Man aind collect a samplle of his…

A: Crossing over is a phenomenon that occurs in the linked genes. When the crossing over occurs between…

Q: im writing an essay about genetic defects that includes one example and an explanaion with it. what…

A: Genetic defects are attributed to the defects in the gene that is the defect that are either due to…

Q: If children obtain half of their Gene's from one parent and half from the other parent, why aren't…

A: A genome of offspring is inherited from both the parents. Half of the genetic material is inherited…

Q: Hemophilia results from a sex-linked gene. The disease is most common in males, but the hemophilia…

A:

Q: For question c1.  I put 47, xxy  I'm not sure  and diagnosis would be trisomy 13 syndrome ?

A: The term karyotype refers to the chromosome complement of a cell. It represents the full set of…

Q: Joe has classic hemophilia, an X-linked recessive disease. Could Joe have inherited the gene for…

A: Genes carry coded genetic information in the form of specific nucleotide sequences. This specific…

Q: If we call the amount of DNA per genome “x,” name asituation or situations in diploid organisms in…

A: Introduction: Amount of DNA varies in the cell according to the phase it is in with respect to the…

Q: What do you mean by homozygous condition for a gene?

A: Crossing over is defined as the process of exchange of chromosomal segments between the no sister…

Q: are forms of the same gene with small differences in their sequence of DNA. Alleles A O Histones .B…

A: Alleles are forms of the same gene with small difference in their sequence of DNA So, the correct…

Q: A single syndrome that has more than one genetic causeexhibits ________.a. pleiotropyb. incomplete…

A: A single syndrome that has more than one genetic cause exhibits pleiotropy.

Q: Which of the following describes the pattern of sex chromosomes in this athlete? (Look at picture)…

A: Klinefelter syndrome is characterized by the presence of one extra X chromosome in a male. Many…

Q: An organism is described as Rr, with red coloring. Rr is the organism’s________ , while red color is…

A: Sir Gregor Mendel was a priest and a teacher who did the famous hybridization experiment on garden…

Q: A shows the number and appearance of homologous chromosomes. O a. Karyotype O b. Phenotype Oc.…

A: The compact string-like structure composed of deoxyribonucleic acid and special histone protein is…

Q: The gene for polydactyly (P) is autosomal and dominant to normal fingers (p). Hemophilia is…

A: Genes are specific regions in the DNA that code for specific proteins. The genetic instructions…

Q: A 31 year old woman consults her physicain because she is concerned about developing breast cancer.…

A: Abnormal and uncontrolled growth and proliferation of cells with a capacity to invade other healthy…

Q: One of the forms of rickets is inherited in the autosomal dominant way. This disease is a result of:…

A: A disease in which the bones of children start to weaken and soften is known as Rickets. Mostly it…

Q: Under the influence of gamma-radiation a fragment of the chromosome was lost. What chromosomal…

A: In case of deletion lods of one or more nucleotide from a segment of DNA occur. In case of…

Q: An example of a single gene disorder is O a. Cri-du-chat Syndrome O b. Phenylketournia Patou

A: Cr-du-chat Syndrome : It is a rare genetic disorder which is caused by a missing section on a…

Q: Which of the following events or processes can result in Patau syndrome, Turner Syndrome, or…

A: The gene is the basic unit of heredity. Most of the organisms have Deoxyribonucleic acid (DNA) as…

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: d Dd 501. s0% 5. Another type of blood disorder is hemophilia, which is an X linked disorder caused…

A: Hemophilia is a sex linked recessive disorder.

Q: A couple planning their family are aware that through the pastthree generations on the husband’s…

A: The karyotype banding analysis is the test that is done in a person's DNA for finding the normal and…

Q: Cystic fibrosis is a genetic disorder that damages the tissues of the lungs. A- normal a - afflicted…

A: Introduction Sir Gregor Mendel is known as Father of Genetics. He was the pioneer scientist who…

Q: Genes are located in the chromosomes of cells, with each pair containing two variants called Each of…

A: Genetics is the subdomain of biology that deals with the heredity, genes, genetic variations, and…

Q: tl ban o a rne dononant allo le dD), ifs dccessrveallele (h) produces aght bour Another gene has wo…

A: Epistasis is the phenomenon when two or more than two genes contribute to a particular phenotype. In…

Q: Someone has 3 chromosomes instead of two is a _____________ Person.

A: A trisomy is a chromosomal condition characterized by the presence of one extra copy of chromosome.…

Q: Which mutation, if it occurred in an individual’s mother, could be passed on to her child?

A: The type of mutation which is passed on to the child from their parents is called a hereditary…

Q: There are six types of agglutinogen named C,D, E and c,d,e.the first three are dominant and last…

A: In blood typing, antigens on the surfaces of red blood cells (RBCs) are known as agglutinogens.…

Q: A 14-year-old girl has some abnormalities: her height is lower than that of the girls of the same…

A: Chromosomal disorders are caused due to absence or excess or abnormal arrangement of one or more…

Q: If Mr. Kennedy dyes his hair hot pink, he has changed his O alleles O genes O genotype O phenotype O…

A: According to the given options, DNA is a nucleotide sequence which is the genetic material of an…

Q: wo individuals have a mutation on chromosome 18. This mutation, when present in one copy, results in…

A: A mutation can be defined as the change in the DNA that results in change or damage in the gene.…

Q: Identify the type of chromosomal abnormality shown here: O inversion O deletion O insertion O…

A: Chromosomes are filamentous bodies present in the nucleus. They are self-replicating and play an…

Q: It is the process where the parent's gene pairs separate.

A: Separation of different traits of the same gene or allele pair during meiosis so that they can…

Q: What is the genetic phenomenon when a person has a specific genotype but phenotypically presents…

A: Genotype is defined as the genetic constituent of an organism. where is the phenotype is defined as…

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: 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: Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children…

A: Mutations in the LMNA gene cause Hutchinson-Gilford progeria syndrome. Here, we have to select the…

Q: Hello, good day. I have a problem answering this question, and I need your help. Hoping for a…

A: DNA is stands for Deoxyribonucleic acid.It is a genetical material present in all peoples.Every…

Q: How can having the heterozygous form of the Tay Sachs genotype be a blessing? O It may protect…

A: The heterozygous form of the Tay Sachs genotype, It may protect against TB.

Q: A female born with Angelman syndrome carries a deletion in theAS gene (i.e., the UBE3A gene). Which…

A: Angelman syndrome: It is a genetic disorder which is caused seizures, intellectual disability,…

Q: Should an individual’s genetic information ever become public information?

A: Bioethics is related to medical policy, research and practices moral judgment. It works on four…

Q: How many chromosomes are there in the somatic cells of a newborn boy with: a. The cri-du chat…

A: Chromosomes are responsible for our inherited characteristics . Any abberation in chromosome no. Or…

Q: Jeremiah Kingman and his wife have child. Jeremiah's phenotype is Rzr' and his wife's phenotyp is…

A: Phenotype is defined as the physical appearance of an individual for any particular trait , it…

Q: Using punnet square, in case of autosomal recessive mutation, determine the chances of a carrier…

A: Mutation is the change in our DNA base pair sequence due to various environmental factors such as UV…

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.