13) Use the image below of the X and Y sex chromosomes of a human to answer the following question. Which of the following statements is true? A) This person is a female with Haemophilia. B) This person is a male with Ocular Albinism. C) This person is a female with Ocular Albinism. D) This person is a male with no sex linked genetic disorders. X Ocular albinism Duchenne muscular dystrophy Androgen insensitivity Severe combined immunodeficiency Haemophilia Colour blindness YDD SRY Sex determination. AZF Sperm development

Q: 15- A woman carries the testicular feminization mutation (tfm) on one of her X chromosomes: the…

A: Partial androgen insensitivity (PAIS) is a genetic disorder and it affects the male fetus sexual…

Q: Please write in digital format Define the following terms: a) Triploid b) Monosomic c) Trisomic d)…

A: Normal cell has a diploid number of chromosomes. Each cell has 23 pairs of chromosomes out of which…

Q: Red-green color blindness is X-linked recessive. A woman with normal color vision has a mother who…

A: Given: Red-green color blindness is X-linked recessive. Women, mother is color blind - XhXh Woman…

Q: Which of the following statements is true regarding the inheritance of a human X-linked recessive…

A: A recessive trait is the trait that expresses only when present in 2 copies i.e expresses only when…

Q: What do you mean by translocation?

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

Q: 3. STATEMENT: Color-blindness is due to a sex-linked recessive gene. A colorblind man marries a…

A:

Q: What are the Human Health Effects of each(Tetramethrin and Lambda-Cyhalothrin) ? Most likely…

A: Lambda-cyhalothrin - Lambda-cyhalothrin is a kind of synthetic pyrethroid insecticide that is used…

Q: A woman who is eight (8) weeks pregnant requests a direct test for Huntington’s disease on her…

A: Huntington's disorder is an autosomal dominant genetic disorder. It causes the breakdown of the…

Q: Nondisjunction can occur at either the first or second division of meiosis. XXY individuals could…

A: When homologous chromosomes or sister chromatids fail to separate properly during cell division, is…

Q: Mr. and Mrs. Smith, both 40 years of age, are healthy with no knowngenetic conditions. Their newborn…

A: Down syndrome is defined as the condition in which an individual contains an extra chromosome. In…

Q: Please explain Androgen Insensitivity Syndrome (ALS). What is the phenotype of these individuals?…

A: The common etiology of aberrant sexual development, androgen insensitivity syndrome, results in a…

Q: 8 9 10 11 12 13 14 15 16 17 18 ir 19 20 21 22 (8) Fig. 6-3, p.123 N CITE

A: Karyotyping is a test to examine chromosomes in a sample of cells. This test can help identify…

Q: nd explain it using the following headings: O Name of disorder ) type of variation in chromosome…

A: When a cell is not dividing, chromosomes are not visible in the nucleus, even under a microscope.…

Q: Genetic Markers are___Portions of a ___whose inheritance patterns can be followed A) unidentifiable,…

A: Genetic markers can be described as DNA sequences whose positions on chromosomes are predefined.…

Q: A woman with no phenotype is known to have a 14:21 translocation. Please answer questions 1 and 2.…

A: Between two acrocentric chromosomes where the centromere is at one end of the…

Q: A man with blood type A (whose mother was blood type O) has children with a woman that has blood…

A: The correct option is (C).A man is heterozygous for blood group A as his mother was blood type O.…

Q: The body cells of chickens have 78 chromosomes in their nuclei. (i) State the number of chromosomes…

A: The indirect process of cell division in which the chromosomes of parent cells divide once, but…

Q: a) What is the chromosomal abnormality associated with Fragile-X Syndrome?   b) What is the…

A: Fragile X syndrome is a genetic condition which causes many problems in development.

Q: Why must the carrier of a genetic disease be heterozygous?

A: Homozygous means a person carries two identical pair of the gene whereas heterozygous means the…

Q: How many Barr bodies are present in the interphase cells of the ff. individuals? A) Klinefelters…

A: A Barr body is an inactivated X chromosome present in female somatic cells, named after discoverer…

Q: a) Are X-linked recessive human genetic disorders more common in males or females and why?   b)…

A: X-linked recessive disorders are genetic conditions that are caused by mutations in genes on the X…

Q: An individual has a deletion of part of the short arm of chromosome 5.  This individual also has a…

A: A chromosome is a DNA molecule and part of genetic material.

Q: Pancreatic cancer is clearly inherited as an autosomal dominant trait in the family illustrated in…

A: Cancer is an uncontrolled division of cell that has a defunct apoptosis mechanism. Usually, when…

Q: Which of the following statements is true of a species that has a chromosome number of 2n = 36? a) A…

A: Introduction The DNA molecule is coiled into thread-like structures called chromosomes in the…

Q: 2 3 5 8. 10 11 12 13 14 15 16 17 18 19 20 Y 21 22 (4) © 2006 Brooks/Cole - Thomson Fig. 6-18b, p.135

A: KARYOTYPING It is the process by which photographs of chromosomes are taken in order to determine…

Q: A woman with a balanced reciprocal translocation of Chromosomes 4 and 20 (karyotype, right panel…

A: In a balanced reciprocal translocation genetic material is exchanged between two chromosomes with no…

Q: Select the statements below that are TRUE.   Select 4 correct answer(s) Question 14 options:   A)…

A: This question tests your understanding of various genetic phenomena:Mutations: Spontaneous changes…

Q: Shown below is a karyotype from a human being. How many total autosomes does this individual have?…

A: A chromosome is a long DNA molecule that contains part or all of an organism's genetic material.…

Q: Consider the genetic cross for absent-mindedness, which is a dominant trait. All of the offspring…

A: A dominant trait is an inherited feature that occurs in an offspring when a dominant allele is…

Q: 12. The spindle checkpoint ensures that all chromosomes are attached to the mitotic spindle. If this…

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Genomic studies

Genomic studies (genomics) is the study of the whole genome of an organism. Using bioinformatics and high-performance computing, genomic researchers examined massive amounts of deoxyribonucleic acid (DNA)-sequence data to discover variations or mutations that affect drug response, health, or disease. Genomics is a much younger discipline than genetics, having only emerged in the last few decades as a result of technological advancements in DNA sequencing and computational biology.