Draw a three-generation pedigree of an Autosomal Dominant family, with three children for every mating. Fill in the affected individuals. Then say, could your pedigree also be each of the following other types of pedigrees: Autosomal Recessive, X-Linked Dominant, X-linked recessive, Y-linked, and Mitochondrial. If it cannot be one of these patterns you must say why not and be VERY specific. If it can be, you can just say yes. autosomal dominant autosomal recessive x-linked dominant x-linked recessive y-linked mitochondrial

Draw a three-generation pedigree of an Autosomal Dominant family, with three children for every mating. Fill in the affected individuals. Then say, could your pedigree also be each of the following other types of pedigrees: Autosomal Recessive, X-Linked Dominant, X-linked recessive, Y-linked, and Mitochondrial. If it cannot be one of these patterns you must say why not and be VERY specific. If it can be, you can just say yes. autosomal dominant autosomal recessive x-linked dominant x-linked recessive y-linked mitochondrial

Name: Draw a three-generation pedigree of an Autosomal Dominant family, with
Uploaded: 2024-03-20T06:42:55.000Z
Channel: Bartleby
Description: Draw a three-generation pedigree of an Autosomal Dominant family, with three children for every mating. Fill in the affected individuals. Then say, could your pedigree also be each of the following other types of pedigrees: Autosomal Recessive, X-Lin

Biology: The Dynamic Science (MindTap Course List)

4th Edition

ISBN:9781305389892

Author:Peter J. Russell, Paul E. Hertz, Beverly McMillan

Publisher:Peter J. Russell, Paul E. Hertz, Beverly McMillan

Chapter13: Genes, Chromosomes, And Human Genetics

Section13.2: Sex-linked Genes

Problem 1SB: You have a true-breeding strain of miniature-winged fruit flies, where this wing trait is recessive...

See similar textbooks

Similar questions

Using the pedigree chart attached: Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why?
In the pedigree attached, the shaded symbols represent people affected with a neurological disorder caused by an X-linked recessive allele. The normal allele is D and the recessive allele is d. What are the genotypes of every person in this pedigree? Please explain in as much detail as possible.
What are the genotypes of the mother and father in the pedigree below? The pedigree shows albinism (an autosomal recessive trait). The shaded shapes represent albino individuals. a. mother - homozygous dominant; father - homozygous dominant b. mother - heterozygous; father - homozygous recessive c. mother - homozygous recessive; father - heterozygous d. mother - heterozygous; father - heterozygous e. mother - homozygous dominant; father - homozygous recessive
Consider an autosomal dominant trait with reduced penetrance and complete expressivity. What might you expect to see on a pedigree diagram for a family with all affected individuals may not have an affected parent (the trait appears to skip generations). more than one of the options listed here affected males always pass the trait to daughters but never to sons only one sex displays the trait all affected individuals have an affected parent (the trait does not appear to skip generations)
For the pedigree shown here, the disorder is caused by a recessive (g) autosomal allele. Label each of the following individuals with the correct genotypa. Generation I, number 2 b. Generation II, number 1 c. Generation II, number 2 d. Generation III, number 3
If Subject 1 in the pedigree shown below is heterozygous for a rare autosomal recessive disease, what is the likelihood that Subject 7 will inherit the disease? 1/2 1/4 1/8 1/16 1/32 1/64 0
The following pedigree describes the inheritance of Lesch-Nyhan syndrome, an x-linked recessive disease. Affected individuals are shaded. what is the probability, that the indicated child (IV.1) will be affected by Lesch-Nyhan syndrome? show solution
Assume that a particular unusual phenotype is caused by an autosomal recessive allele. John marries Jane, and they have a daughter Mia together who has the unusual phenotype. John has a brother Carlos who appears normal. Jane has a sister Margit with the unusual phenotype. John and Jane are not related, and none of their parents have the unusual phenotype. Draw a 3-generation pedigree that depicts the entire scenario and assign the most likely genotypes to each individual. (You can use any letter you wish to represent the gene.) Yes, you should include Jane's parents and sister, and also John's parents and brother, as part of the pedigree. And don't forget Mia!
Which of the following is indicated by roman numerals in a pedigree? a.Presence of the studied trait b.Generation c.Sex d.Marriage status Which of the following disorders in humans has an autosomal dominant inheritance pattern? a.Albinism b.Hemophilia c.Tay-Sachs disease d.Huntington’s disease For an X-linked recessive allele, what proportion of female offspring will be carriers in the cross of an affected father and a noncarrying mother? a.50 percent b.0 percent c.100 percent
Above is a pedigree for colorblindness. Based on the pedigree, is the disease dominant or recessive and is it sex-linked or autosomal? Why? Furthermore, what is the probability that 18 on this chart is affected but the condition, and what is the probability that 18 is a carrier? Why? Are the probability of being a carrier and an affected individual different? Why
We know that the most common form of color blindness results from an X linked recessivegene. A couple with normal color vision has a daughter with normal vision and a son who is colour-blind. What is the probability that the daughter is a carrier for the colour-blindness allele? Draw punnet square/pedigree to support your results.
In mice the autosomal genotype yy is for gray fur, YY is for brown fur and Yy is for yellow fur. What is the ratio of offspring from the cross between a brown mouse and a yellow mouse? ABO blood groups, an autosomal trait, in Humans are genetically determined. A woman with type O blood has a son with type O. What are the possible genotype(s) of the son, his mother and possible father? Mother: Father: Son: Polydactylism (extra digits) is due to a dominant autosomal allele, what is the likelihood that a couple with the normal number of digits have a son with polydactylism? Flower color in snapdragons is due to a gene with incomplete dominance: CRCR plants have red flowers, CRCW have pink flowers, and CWCW plants have white flowers. Which cross is expected to yield progeny that all have pink flowers? A couple is expressing a child, the man has hemophilia (a sex-linked blood disorder due to a recessive allele) and the woman is a carrier…