Biology 2e
2nd Edition
ISBN: 9781947172517
Author: Matthew Douglas, Jung Choi, Mary Ann Clark
Publisher: OpenStax
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Textbook Question
Chapter 13, Problem 11RQ
The genotype XXY corresponds to
- Klinefelter syndrome
- Turner syndrome
- Triplo-X
- Jacob syndrome
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AaBBdd x AaBbDd
punnet square
genotype
phenotype
AaBbDd x AaBbDd
Punnet square
Phenotype
Genotype
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hilia is an inherited genetic disorder linked to the
nosome that results in ineffective blood clotting when a blood
is damaged. The most common type, hemophilia A, occurs
5000 male births. Any male who carries the gene will express
enotype. Hemophilia is extremely rare in women.
Parents
Carrler
female
Normal
male
couple wish to have children. The woman knows she a
rrier for hemophilia. The man is not a hemophiliac. Use
e notation Xh for hemophilia and XH for the dominant
ele to complete the diagram on the right including the
arent genotypes, gametes and possible fertilizations.
rite the genotypes and phenotypes in the table below.
XY
XhXh
Gametes
Xh
Xh
Genotypes
Phenotypes
Possible
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Male
children
XhY
Xhx
XhY
XhX
Paternal gametes
Paternal gametes
Female
children
00
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A second couple also wish to have children. The
woman knows her maternal grandfather was a
hemophiliac, but neither her mother or father were.
Determine the probability she is a carrier…
Chapter 13 Solutions
Biology 2e
Ch. 13 - Figure 13.3 In a test cross for two...Ch. 13 - Figure 13.4 Which of the following statements is...Ch. 13 - Figure 13.6 Which of the following statements...Ch. 13 - X-linked recessive traits in humans (or in...Ch. 13 - The first suggestion that chromosomes may...Ch. 13 - Which recombination frequency corresponds to...Ch. 13 - Which recombination frequency corresponds to...Ch. 13 - Which of the following codes describes position 12...Ch. 13 - In agriculture, polyploid crops (like coffee,...Ch. 13 - Assume a pericentric inversion occurred in one of...
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Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Similar questions
- The genotype XXY corresponds to: a. Klinefelter syndrome b. Turner syndrome c. Tripto-X d. Jacob syndromearrow_forwardDoes this individual display any genetic disorders?arrow_forwardWhat is the most likely mode of inheritance for the disease depicted in the following pedigree? I II III 1 1 2 1 2 autosomal recessive autosomal dominant 3 3 2 4 4 5 5 6arrow_forward
- Given the karyotype shown at right, is this a male or a female? Normal or abnormal? What would the phenotype of this individual be?arrow_forwardComplete this mendelian gentics chartarrow_forwardMarfan syndrome is transmitted by a dominant gene.State the probability that a child with an affected parentwill have the disorderarrow_forward
- /d/1n5NtidRwTwUzcDkDPi5Z9P_SHPZ91A-XH-pfftLbhNc/edit (1) O pols Add-ons Help Last edit was seconds ago BIUA ミ: 12 + ext Calibri I|1 6 I 2 Section 5: Trihybrid cross and Laws of probability For a trihybrid cross, in which inheritance of alleles for three genes is tracked, drawing a Punnett square that combines all three genes may not be practical. Instead the laws of probability may be used. The product law of probabilities says that when alleles for separate genes segregate independently, we can figure out the probability of a particular combined genotype by multiplying the probability of the alleles for each gene. 13. We cross a homozygous tall pea plant with yellow, round seeds to a homozygous dwarf pea plant with green, wrinkled seeds. All the F1 offspring are all tall plants with yellow, round seeds. a. What are the expected F2 ratios (use fractions) of tall and dwarf plants? b. What are the expected F2 ratios (use fractions) of yellow and green seeds? C. What are the expected F2…arrow_forwardHow many Y chromosomes are there in an individual with Klinefelter syndrome? 0 1 2 3 4 CHOOSE ONEarrow_forwardWhat pattern does the genetic disorder follow?arrow_forward
- Paste or draw a picture of a Punnett square showing a cross between an individual with the disorder and a person who is homozygous dominant for the allele that causes the sickle cell anemia disorderarrow_forwardPlease draw a punnett square for thisarrow_forwardA female with genotype IBi has a child that has blood type O (genotype ii). Which of the following genotypes could the child's father have? Select all correct answers. ii IAIB IAi IBIBarrow_forward
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