11. What is the probable mode of inheritance for the trait in the pedigree below?Examine the pedigree below.IMPTO2Figure 12-3sex linkautosomal dominantHOmultiple allelesautosomal recessive

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Description: 11. What is the probable mode of inheritance for the trait in the pedigree below?Examine the pedigree below.IMPTO2Figure 12-3sex linkautosomal dominantHOmultiple allelesautosomal recessive

The pedigree is a kind of family tree which depicts a mode of inheritance of a particular trait.

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11. What is the probable mode of inheritance for the trait in the pedigree below Examine the pedigree below. www IV 1 Figure 12-3 2 sex link autosomal dominant ПО multiple alleles autosomal recessive

11. What is the probable mode of inheritance for the trait in the pedigree below Examine the pedigree below. www IV 1 Figure 12-3 2 sex link autosomal dominant ПО multiple alleles autosomal recessive

Biology 2e

2nd Edition

ISBN:9781947172517

Author:Matthew Douglas, Jung Choi, Mary Ann Clark

Publisher:Matthew Douglas, Jung Choi, Mary Ann Clark

Chapter12: Mendel's Experiments And Heredity

Section: Chapter Questions

Problem 10RQ: The observable traits expressed by an organism are described as its. phenotype genotype alleles...

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1. Construct a pedigree chart of the trait traced in the situation below.2. The pedigree chart must be constructed with the names and genotypes at the bottom of every individual in the chart.If it is autosomal: Always use the first letter of the dominant trait to represent the dominant allele. For example, if the dominant trait is red, so the allele R-red, while r-yellow. For example, if the person is homozygous dominant for curly hair, we write CC as his genotype. If sex-linked, do not forget to write the parents’ chromosomes (XX-female, XY-male), with their corresponding superscripts (dominant or recessive). The superscript must be based on the first letter of the disorder. For example, the mother is a carrier of hemophilia (which is x-linked recessive), so we write XHXh. If the father has hemophilia, we write XhY. Put the pedigree chart using code properly. The situation is given below: Trait: NeurofibromatosisThe dominant form is neurofibromatosis, caused by the production of…
1. Construct a pedigree chart of the trait traced in the situation below.2. The pedigree chart must be constructed with the names and genotypes at the bottom of every individual in the chart.If it is autosomal: Always use the first letter of the dominant trait to represent the dominant allele. For example, if the dominant trait is red, so the allele R-red, while r-yellow. For example, if the person is homozygous dominant for curly hair, we write CC as his genotype. If sex-linked, do not forget to write the parents’ chromosomes (XX-female, XY-male), with their corresponding superscripts (dominant or recessive). The superscript must be based on the first letter of the disorder. For example, the mother is a carrier of hemophilia (which is x-linked recessive), so we write XHXh. If the father has hemophilia, we write XhY. Put the pedigree chart using code properly. The situation is given below: Trait: NeurofibromatosisThe dominant form is neurofibromatosis, caused by the production of…
1.Why are punnet squares a useful model for studying traits and genetic disorders? 2.Make a dihybrid cross Punnett square for the dihybrid cross YyRr and yyrr.
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1. Hereditary deafness in dalmations (d) is a recessive trait. What percentage of the progeny of crossing DD × Dd will be expected to be a carrier of the deafness allele, but not deaf? (enter a number only) 2.In snapdragons, a flowering plant, red (R) flower colour is dominant to white (r). The heterozygous condition results in pink flower colour. If a two pink flowered snapdragons are crossed, what is the resulting phenotype ratio? Select one: a.2:2 b.1:1:1:1 c.1:2:1 d.3:1 e. (all will be the same)