Answer:
1) a. in more males than in females ( Human body is made up of cells. Every cell in the human body contains chromosomes. Male's cells contain both one X and one Y chromosomes. Female's cells contain two X chromosome. If any disorder related to the X chromosome, it mostly affects male because the male has only one X chromosome while the female has two.)
2) c. vulnerability ( Because of the biological structure of the human body, It is very sensitive to the environment so that it has a high possibility to become ill. This innate disability is called vulnerability)
3) c. Consciousness will not be capable of explanation using material explanations. (Non-material neuroscientists see the problem from the spiritual stage. They concern about the soul. That's why they believed that by using material explanation we can't understand about soul/consciousness)
4) B. a genetic predisposition which may lead to the production of the disorder. ( Basically genes have the inability to resist disorders in some people. That's why there is a high possibility to get the disorder. This is called vulnerability for a specific disorder)
Question 1 ips A genetic disorder that is associated with the X-chromosome will likely appear in...
Q1. Based on a 2014 report from a consortium called GIANT (Genetic Investigation of Anthropometric Traits), it has been reported that there are at least 424 genes that contribute to determining the polygenic trait, height, in humans. Assuming there are two alleles for each gene, how many unique phenotypes would be generated? U ow 424 425 848 849 6.023 x 10 Q2. In fruit flies, the y+ and ct+ genes are located on the X chromosome. Grey body color is...
9. Different genes are located on different kinds of genetic elements - autosomes, W chromosomes, the mitochondrial genome, etc. Different elements are inherited in different ways, so different offspring inherit different elements from different parents. For each case, answer "both parents', 'mother', 'father, or 'neither parents. For instance, sons inherit autosomal genes from both parents, but sons inherit W chromosome genes from neither parent (because males are ZZ, and don't have a W chromosome...) (1 point per answer) Sons inherit...
ANSWER ALL QUESTIONS Questions 7-8: The figures below are a pedigree analysis of a genetic disorder called small foot, and the corresponding molecular analysis of the small foot gene - associated Mstl-RFLP markers of Mary's family. Mary is individual 3. Parents Siblings NORMAL Each individual's small foot gene DNA was amplified, and digested with Msti. 1000 bp 400 600 600 bp 1 23 45 nividual PCR, Mst1 Digest DISEASE 400 bp A. The molecular summary of the small foot gene...
1. Describe two kinds of recombination in eukaryotes. True of False 2._____ A recessive phenotype can be expressed by some progeny of a monohybrid cross. 3._____ Epistatic genes may result from dominant or recessive alleles. 4._____ At a single locus, a diploid individual may have more than two different alleles. 5. _____ A temperature-sensitive allele is an example of a genotype x environment interaction. 6. _____ All of the genetic material in a eukaryotic cell is found in the nucleus....
7.) Haemophilia is an X-linked recessive disorder. If a male haemophiliac mates with a normal (non-haemophiliac) homozygous woman, would the progeny be affected? a. All males would be carriers. All females would be normal. b. All males would be normal. Half of the females would be carriers and half of the females would have haemophilia. c. All males would be normal. All females would be carriers. d. Half of each sex would be normal and half of each sex would...
Please help with this genetic question. If possible, show work. Thank you ! Question 29 0/2 pts Two unlinked, epistatic genes regulate production of flower pigments in diploid sweet peas, as shown in the metabolic pathway below. Each gene codes for the production of an enzyme, and each gene has two possible alleles-dominant and recessive. Plants with at least one dominant R allele will produce the blue pigment. Plants with at least one dominant R allele and at least one...
exercise 6 pre lab mendallion and human gametes QUESTION 1 Select the term described An allele expressed only in the absence of a dominant allele Term for genes that behave predictably In F2 generations One variety of a gene there may be many varletions in a population Using pollen from a different plant to another plant A genetic map of traits overal gener offspring of two parents with different trait Using pollen (sperm from the same plan own egg The...
Genetics question!! Please help with these 3. Thanks A woman with Turner syndrome (X0-only one X-chromosome) is also colorblind (an X-linked recessive phenotype). Both of her parents have normal color vision. This women's karyotype and genotype could have arisen by: a) a mutation in her mother's X-chromosome b) non-disjunction in mitosis c) non-disjunction in meiosis 1 in her father d) non-disjunction in meiosis 2 in her mother e) non-disjunction in meiosis 1 in her mother 10. Mitochondrial genomes a) replicate...
please help with Q. 9, 22, 59, 72. thanks! Bookmarks People Tab Window Fra * Q Genetica Fral *1 ses/213459/quizzes/255809/take Help What are the typ * Q Fram Stud Pashcards - Be * Q D Question 9 1 pts Which of the following in determining the phenotype for the ABO blood system is correct? A. Ois dominant over A Ais dominant over B O is recessive Bis dominant over A D Question 10 1 pts Two phenotypically normal individuals have...
Name Sex-linked traits are genetic char segments of DNA found on chromosomes that Sex-Linked Traits Senetic characteristics determined by genes located on sex chromosomes. Genies are and on chromosomes that carry information for protein production and that are sponsible for the inheritance of specific traits Genes exist in alternative forms called alleics. or a trail is inherited from each parent Like traits originating from genes on autosomes (non-se chromosomes), sex-linked to omosomes), sex-linked traits are passed from parents to offspring...