List the type of heredity (ie autosomal dominant and recessive, X-linked dominant and recessive, epistasis, polygenic, codominant) for color blindness, ABO Blood types, Rh factor, nail patella syndrome, Fragile X syndrome, Kleinfelter syndrome, Turner syndrome, Trisomy 21, CAIS, albinism, PKU.

List the type of heredity (ie autosomal dominant and recessive, X-linked dominant and recessive, epistasis, polygenic, codominant) for color blindness, ABO Blood types, Rh factor, nail patella syndrome, Fragile X syndrome, Kleinfelter syndrome, Turner syndrome, Trisomy 21, CAIS, albinism, PKU.

Name: List the type of heredity (ie autosomal dominant and recessive, X-link
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Description: List the type of heredity (ie autosomal dominant and recessive, X-linked dominant and recessive, epistasis, polygenic, codominant) for color blindness, ABO Blood types, Rh factor, nail patella syndrome, Fragile X syndrome, Kleinfelter syndrome, Turne

Biology (MindTap Course List)

11th Edition

ISBN:9781337392938

Author:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Publisher:Eldra Solomon, Charles Martin, Diana W. Martin, Linda R. Berg

Chapter16: Human Genetics And The Human Genome

Section16.3: Genetic Diseases Caused By Single-gene Mutations

Problem 7LO: State whether each of the following genetic defects is inherited as an autosomal recessive,...

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In 1-3 sentences define the following heredity types: Autosomal dominant and recessive, X-linked dominant and recessive, epistasis, polygenic, codominant
Y-linked Amelogenesis imperfecta (A), a congenital disorder that affects the formation of the teeth enamel making affected individuals at higher risk for dental cavities and related problems. X-linked dominant hypophosphatemia (H), a form of rickets or vitamin D deficiency that affects the bones which causes pain, osteoarthritis, and abnormal shapeabnormal shape. X-linked recessive progressive Duchenne muscular dystrophy (m), a muscular disorder, leading to an irreversible gradual wasting of skeletal muscles. Hannah, the same as her mom, is heterozygous for both X-linked traits. While her dad is suffering from both muscular dystrophy and hypophosphatemia. Hannah's husband, Joey has a mom suffering from musculardystrophy regardless of having normal bone conditions. His dad has been blessed with strong muscles and bones, however, he is suffering from amelogenesis imperfecta. What are the complete genotypes of each person?a. Joey's momb. Joey's dadc. Joeyd. Hannah's mome. Hannah's dad f.…
reference text Ph.D Fernando, Harvard Professor of Genetic Epidemiology, knows a thing or two about Twins. He must know as he is head of the Twin Research Department where he works with about 3,500 pairs of identical twins, researching the influence of a person's genes on everything from the probability of being obese, whether or not they have religious beliefs, and, how, do they fall into sentimental issues. Anyone who is a twin, or who has ever met a pair of identical twins, can attest to how remarkably similar they are to each other, even in the rare cases of adopted twins raised in separate homes.A recent article begins with an introduction to two middle-aged twin sisters called Susan and Polly, one of the pairs of twins in the study group of the Department of Research of Harvard. Although they were treated almost as a single person growing up, with cuts from identical hair and clothes, the twins began to diverge in their teens as they they gained the freedom to make their own…
Complete a new Punnett Square below, for a woman who is a carrier for sickle cell, who is married to a man who has normal hemoglobin and is homozygous. A carrier for a recessive trait has a heterozygous genotype that "carries" the recessive allele without expressing it, since the dominant allele is expressed. Women or men can be carriers of traits on non-sex chromosomes, or autosomes. What are the possible genotypes that you can identify, do any of the possible genotypes result in sickle cell anemia, and what is the chance that any of the offspring are carriers for sickle cell anemia?
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Please Answer with reason: When counseling parents about genetic transmission of an X-linked disorder, which concept does the nurse keep in mind? a. An X-linked disorder can be traced through the paternal lineage. b. A female can only pass an X-liked disorder to a son c. A male can pass an X-linked mutation to a son or a daughter d. A male with a mutation in an X-linked gene will manifest the disease. 5) The nurse explains to parents that if both of them are carriers of an autosomal recessive genetic mutation, the chance of each child NOT inheriting the disease (affected) is a. 25% c. 0% b. 75% d. 50%
Complete a new Punnett square below, for a woman who is a carrier for sickle cell, who is married to a man who has sickle cell. What are the possible genotypes that you can identify, what is the ratio of phenotypes that are possible, and what is the chance that any of the offspring are affected by sickle cell anemia?
Given: Father - heterozygous for the H locus of the H antigen, heterozygous for the B locus of the ABO blood group system, heterozygous for the D locus of the Rh blood group system, and deuteranope Mother - heterozygous for the H locus of the H antigen, heterozygous for the A locus of the ABO blood group system, heterozygous for the D locus of the Rh blood group system, and carrier for the trait deuteranopia Task: Using the line fork method, determine the probabilities in ratio form of all possible phenotype combinations of the traits in the biological offspring of the couple. Include the solution
For the Y-linked gene, use T for hypertrichosis. For X-linked genes, use the letters H for blood trait and E for eye trait. Krisha, a carrier of the genes for hemophilia and colorblindness, is married to Kyle who is color blind, having normal red blood cells. Veronica (Krisha & Kyle's daughter), turned out to be a carrier for both genes. Julian has hypertrichosis and is married to Josie. Both do not exhibit any allele for color blindness and never had any history for hemophilia. Bernard (Julian & Josie's son) will be married to Veronica. What are the complete genotypes of the following persons: a. Krisha b. Kyle c. Veronica d. Julian e. Josie f. Bernard g. Josie & Bernard's baby
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A woman homozygous for normal height, with freckles, almond-shaped eyes, small nose, and Type A blood, has a Type O mother with no freckles and a type AB father with round eyes. She is engaged to a man with achondroplasia, round eyes and medium sized nose. Unlike his father, hismother is of normal height. Both his parents have Type O blood but nobody from both sides of his family has or had freckles. a. Write the COMPLETE genotypes of the man and the woman. Clearly indicate which genotype belongs to whom. b. Based on their genotypes, what is the probability that they will have: b.1 a child with Achondroplasia? b.2 a child of normal height? b.3 a child with type AB blood? b.4 a daughter with round eyes, freckles, and medium sized nose? b.5 a son with almond eyes, no freckles, and small nose?b.6 a daughter with same genotype as the woman? b.7 a son with same genotype as the man?