please help me with this question Short Answer 3. The pedigree shown is of a family with an X-linked recessive disease. The sex chromosomes are indicated. Individual II-2 is the result of a non-disjunction event in one of the parents.12XHXH xhy112IIXhY B) Upon further testing, it is discovered that Individual l-1 has a mild case of the disease. Please give a short explanation as to how that is possible.

The X-linked recessive disorder is a genetic condition in which mutations in genes are present on…

Answered: B) Upon further testing, it is…

B) Upon further testing, it is discovered that Individual I-1 has a mild case of the disease. Please give a short explanation as to how that is possible.

Biology 2e

2nd Edition

ISBN:9781947172517

Author:Matthew Douglas, Jung Choi, Mary Ann Clark

Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark

Chapter13: Modern Understandings Of Inheritance

Section: Chapter Questions

Problem 11RQ: The genotype XXY corresponds to Klinefelter syndrome Turner syndrome Triplo-X Jacob syndrome

See similar textbooks

Related questions

Q: A student performed a plaque assay and noticed that the plaques formed were very small. In a few…

A: The environment is full of various organisms. These might be unicellular or multicellular. The…

Q: Why this term is used - malignant ?

A: Malaignant term used in cancer.

Q: What is the likely mechanism of spread of NDM-1?

A: NDM-1 is the protein product of a gene that some bacteria produce. A bacterial strain containing…

Q: For each of the E. coli strains containing the lacoperon alleles listed, indicate whether the strain…

A: The lac operon is a type of inducible operon, which uses lactose as the source of energy. It gets…

Q: What is Interleukin 1 (IL-1)?

A: The immune system has a vital role in protecting the body from outside pathogens (bacteria, viruses,…

Q: According to Research and Development department analysis results, it was concluded that a two-stage…

A: a) They chose 2 stage approach because this 2 stage strategy involves division of plasma cell…

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: Classify hyperlipoproteinemia.

A: Hyperlipoproteinemia is a disorder where the body is unable to break down lipids or fats in the…

Q: Southern Blotting & Detection of sickle cell disease: - Please label the figure and discuss each…

A: Sickle cell is an autosomal recessive disorder and caused by mutation in codons that code for the…

Q: List seven factors that suggest a disease may have a genetic component.

A: DNA is the genetic material in most living organisms. It is the information hub of the cell that…

Q: Explain the connection between the founder and the G8-C marker.

A: In this example the original mutation that caused the huntington allele occurred in a germline cell…

Q: In response to the following question, write a sentence outline and one bodyparagraph. using cause…

A: Covid 19 It is a viral disease caused by novel corona virus (SARS-CoV-2 that is severe acute…

Q: What is the pathogenesis of Isolated IgA Deficiency? Please provide flow chart

A: Immunology is a section of biology that includes the study of molecules, cells, and organs that…

Q: Rewrite the following sentences after correction. The N1303K mutation in the CFTR gene of CF…

A: Since you have posted multiple independent questions in the same request, we will do the first…

Q: "Genome-Wide Association Studies Identify Genome Variations That Contribute to Disease" Explain this…

A: The genome-wide association comprises scanning all the marker genomes or complete sets of DNA to…

Q: Which of the IgG subclasses would you think was in principle most desirable for use as a therapeutic…

A: The antibodies formed by the immune system of the body are referred to as immunoglobulins. These are…

Q: Develop a test where IgG is characterized based on its physical, chemical, or biological properties.

A: Antibody: This can be defined as a protein molecule that is produced by the immune system in…

Q: Please explain the Warburg Effect and how it is used to detect tumors.

A: Warburg effect is phenomenon commonly used to detect the cancerous cells. The detection of cancer…

Q: What is the role of Ku70/80 in direct repair of DSBs?

A: DNA repair is a collection of processes by which a cell identifies and corrects damage to DNA…

Q: Alpha Variant = Lineage B.1.1.7 = UK Variant Beta Variant = Lineage B.1.351 OR 501Y.V2 = South…

A: Viruses such as SARS-CoV-2 evolve throughout time when changes in the genetic code (genetic…

Q: What is the pathogenesis of Isolated IgA Deficiency?

A: NOTE : SIgAD means Selective Immunoglobulin A Deficiency The exact pathogenesis of SIgAD is still…

Q: which gene is mutated in type la maple syrup urine disease?

A: Maple syrup urine disease is associated with problems with feeding, vomiting, low energy levels in…

Q: What programs or projects were implemented by the government in the Philippines for the prevention…

A: Corona virus, also called as Covid-19 is an infectious disease. It is caused by the SARS-CoV-2…

Q: What are the major differences between HTLV-1 and HTLV-2?

A: HTLV-1 and HTLV-2 (human T-cell leukaemia viruses 1 and 2) have identical genomic structures that…

Q: Which person type O, A, B, or AB is considered a universal donor, and which is a universal…

A: Universal donor is the person who can give blood to any individual & universal recipient can…

Q: About the three following diseases: phenylketonuria (PKU), sever combined immuno-deficiency (SCID),…

A: A disease is a condition of an abnormal structure or function of any part or organ of the body. It…

Q: Why is the one hour bundle in sepsis protocol called the one hour bundle?

A: Sepsis is a life-threatening condition that is manifested by numerous signs, symptoms, hemodynamic,…

Q: Identify the virus responsible for adult T-cell leukemia.

A: Adult T-cell leukemia is a mature T- cell malignancy, characterized by organomegaly, hypercalcemia…

Q: ICD-10-CM, code Z85.020 ( personal history of malignant carcinoid tumor of stomach) is reported as…

A: Carcinoid tumor is a rare tumor that begins in the stomach, intestine and colon, in its malignant…

Q: (a) Why did they choose this two-stage approach? (b) How did they cause the cells to shift from a…

A: B-lymphocytes develop from stem cells in bone marrow, which are the specialized white blood cells…

Q: The spread of the corona virus is now becoming enormous. In your point of view as a senior high…

A: Skilled in science, technology, engineering, and mathematics (STEM) play a vital role in the US…

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: Why do cold sores recur throughout the lifetime of an HSV-1 infected individual?

A: HSV-1 infection of the CNS can have lifelong effects such as permanent temporal lobe damage.After…

Q: Make a list of five preventive measures you and your family continuously practice to stop the spread…

A: Coronavirus disease (COVID-19): is an infectious disease caused by the SARS-CoV-2 virus. The…

Q: In determing Rh group, do you consider the control tube for reading when it shows an agglutination…

A: The system of the Rh blood group is used to classify the blood groups depending on the existence or…

Q: What is the Laboratory diagnosis of influenza A virus subtype H1N1? And what are the Prevention,…

A: Viruses are the infectious agents that belong to a class of parasites. They are smaller than…

Q: What does BCR ABL positive mean?

A: The cancer of the white blood cells is known as Chronic myelogenous leukemia (CML) in medical terms.…

Q: What are the vectors for H5N1 and H1N3?

A: In biology, vector is an organism that does not cause the disease but carries the disease causing…

Q: COVID 19 - cause respiratory distress and/ or intestinal distress?

A: The SARS-CoV-2 virus causes Coronavirus Illness (COVID-19), an infectious disease. The majority of…

Q: The N1303K mutation in the CFTR gene of CF patients is autosomal dominant disorder due to insertion…

A: The N1393K mutating in CFTR gene of CF is autosomal recessive disorder where asparagine to lysine…

Q: As a nursing student how can you contribute to avert the spread and effects of COVID-19?

A: The whole world is suffering from this covid-19 and as per the rules and standards from the…

Q: Retroviral delivery of the gene coding for Combined Immunodeficiency. treats individuals with Severe…

A: Successful gene therapy that is performed with the retroviral vectors neceserily requires robust…

Q: Is there any applicable HCPCS Level II codes?

A: Introduction:- These are codes, mostly for non-medical services like prosthetics and ambulance…

Q: What is the APC payment for HCPCS code 78740? Explain.

A: APC weight 3.94 Conversion factor CF $80.79 Wage Index 0.9445

Q: What are the future diagnostic approaches for Covid-19? Explain at your own words

A: A key priority for COVID-19 diagnostic analysis According to the World Health Organization is the…

Q: What is the most significant difference between prion diseases and other diseases caused by…

A: The prion and amyloid phenomena acquired a more general significance for biology due to the finding…

Question

please help me with this question

Short Answer 3. The pedigree shown is of a family with an X-linked recessive disease. The sex chromosomes are indicated. Individual II-2 is the result of a non-disjunction event in one of the parents.
1
2
XHXH xhy
11
2
II
XhY

B) Upon further testing, it is discovered that Individual l-1 has a mild case of the disease. Please give a short explanation as to how that is possible.

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.

Similar questions

I need help with b, c, d the choices for c) are haploid, diploid or tetraploid the choices for d) are same chromosome, a pair of homologus chromosomes, or two different chromosomes
I need help. the answer choices for both blanks are diploid, haploid or zaploid.
I need some help completing this fill-in-the-blank. Each answer option is bolded and bracketed. 1. The purpose of the AMEL locus is [identification of ethnicity, determination of age, identification of gender], it is located in the [autosomes, sx chromosomes]. Females have only one peak originating from their [X only, Y only, X and Y] chromosomes and males have two peaks originating from their [X only, Y only, X and Y] chromosomes. 2. In the D8S1179 locus, Sophie is [homozygous, heterozygous] for allele with 13 copies. One copy of this allele came from her mother and the other copy came from [Sam or Bill, Sam or Harry, Bill or Harry, Sam Bill or Harry(Either 3)] 3. In the D21S11 locus, Sophie's allele [28, 30] came from the mother and her other allele, 28, came from [Sam only, Bill only, Harry only]. 4. In the D18S51 locus, Sophie's paternal allele came from [Bill only, Bill and Harry, Sam Bill or Harry (Either 3)]. 5. You already know Sam, Bill and Harry are related to one another.…
The white spots in this image represent Barr Bodies. The cells are from a Male cell line. What is the sex chromosome complement of this cell line?
17. Who would be more likely to display a recessive X linked trait (like color blindness) 1. Male because they only have one X chromosome 2. Females because they have two X chromosome 3. Females and males are like display X linked recessive traits with equal frequency
Sex Determination (female genotype XX and male genotype XY) A. What fraction of human offspring receive an X chromosome from the mother? B. What fraction receive a Y chromosome from the father? C. Mr. and Mrs. Jackson have seven boys and one girl. What is the probability that their next child will be a girl?
Including the sex chromosomes, the chromosome number of a normal human cell is ___________ and the chromosome number of this HeLa cell is (look at picture). (Hint: Chromosome number is different from total chromosome count.)
Drop-down menu choices: first - recessive epistasis, dominant epistasis, duplicate dominant epistasis, or duplicate recessive epistasis second - the recessive allele f, the dominant allele F, the recessive allele w, the dominant allele W, either recessive allele, or either dominant allele third - gene W, gene F, or the other gene
Fill in the blanks. Including the sex chromosomes, the chromosome number of a normal human cell is __________ and the chromosome number of this HeLa cell is ___________(Hint: Chromosome number is different from total chromosome count.)
MODIFIED TRUE OR FALSE. In the following items, read each statement carefully. I. In humans and other mammals, biological sex is determined by a pair of sex chromosomes: XX in males and XY in females.II. In the sexual pattern of inheritance, an X-linked pattern will be present and can attached both on the X and Y chromosomes. a. The first statement (I) is correct and the second statement (II) is wrong b. The first statement (I) is wrong and the second statement (II) is correct c. Both statements are correct d. Both statements are wrong MODIFIED TRUE OR FALSE. In the following items, read each statement carefully. I. One important event that happens in Meiosis at Prophase 1 is when crossing over between sister chromatids of non-homologous chromosomes takes place.II. This crossing over is the exchange of genetic material that causes variations among individuals. a. The first statement (I) is correct and the second statement (II) is wrong…
MODIFIED TRUE OR FALSE. In the following items, read each statement carefully. I. Mitosis and meiosis are two cellular process that might be quite similar in terms of stages, but technically, different process that have two different functions. II. As an example, mitosis involves the production of genetically different daughter cells whereas meiosis involves the production of genetically identical daughter cells. a. The first statement (I) is correct and the second statement (II) is wrong b. The first statement (I) is wrong and the second statement (II) is correct c. Both statements are correct d. Both statements are wrong I. The continuity of life from one cell to another has its foundation in the reproduction of cells by way of the cell cycle.II. The cell cycle is an orderly sequence of events in the life of a cell from the division of a single parent cell to produce two new daughter cells and are highly conserved across eukaryotes.…
Parents are rr SuSu* RR susu F1 are : draw a punnet square 4 by 4