I need help with everything please. wwwwwmeadSTUDY GUIDENameNormal,pure dominantfemale2 normal females1 normal male1 male with hemophiliaIn your textbook, read about hemophilia in Section 27:3.1. In the boxes below each of these people, draw the sex chromosomes. Then, on the chromosomeswrite the genes they have for hemophilia. The dominant gene is H. The recessive gene is h.Normal male1 normal female1 normal male1 female with hemophilia1 male with hemophilia2 normal females2 males with hemophiliaFemale withhemophiliaH hH|HH HHhHhhhGENETIC DISORDERS2. Complete the following Punnett squares. Then, match the correct Punnett square with each one ofresult it matches.the following expected results. Write the letter of the Punnett square on the line next to the expectedExpected resultsM XXXXXX XXoXoa4. Describe the condition of hemophilia.DateAX XXXXXXa X a X3. Circle the Punnett squares that show individuals with hemophilia.aaMale withhemophiliaBX XM XXXXX XXoXoaClassCHAPTER 27Ma8Normal,heterozygousfernaleXXXXXXXXX XXXXXXXXXXXa XaX aCMa a Xa161

Name: I need help with everything please. wwwwwmeadSTUDY GUIDENameNormal,pur
Uploaded: 2024-03-20T06:42:55.000Z
Channel: Bartleby
Description: I need help with everything please. wwwwwmeadSTUDY GUIDENameNormal,pure dominantfemale2 normal females1 normal male1 male with hemophiliaIn your textbook, read about hemophilia in Section 27:3.1. In the boxes below each of these people, draw the sex

Inheritance pattern is a type of pattern which determines how traits are passed from parents to next…

Science

Biology

In your textbook, read about hemophilia in Section 27:3. 1. In the boxes below each of these people, draw the sex chromosomes. Then, on the chromosomes write the genes they have for hemophilia. The dominant gene is H. The recessive gene is h. Normal male Normal, pure dominant female 2 normal females 1 normal male 1 male with hemophilia 1 normal female 1 normal male 1 female with hemophilia 1 male with hemophilia 2 normal females 2 males with hemophilia Female with hemophilia 2. Complete the following Punnett squares. Then, match the correct Punnett square with each one of the following expected results. Write the letter of the Punnett square on the line next to the expected result it matches. Expected results H h HHHHH hHhhh GENETIC DISORDERS - Describe the condition of hemophilia. Male with hemophilia 3. Circle the Punnett squares that show individuals with hemophilia. X X WWWWW a Xa a X X XXXXX XX aXaX XXXXX XX X.X.XXXXX a XoXo C a Normal, heterozygous fernale XXXXX M aaa X X XXX

In your textbook, read about hemophilia in Section 27:3. 1. In the boxes below each of these people, draw the sex chromosomes. Then, on the chromosomes write the genes they have for hemophilia. The dominant gene is H. The recessive gene is h. Normal male Normal, pure dominant female 2 normal females 1 normal male 1 male with hemophilia 1 normal female 1 normal male 1 female with hemophilia 1 male with hemophilia 2 normal females 2 males with hemophilia Female with hemophilia 2. Complete the following Punnett squares. Then, match the correct Punnett square with each one of the following expected results. Write the letter of the Punnett square on the line next to the expected result it matches. Expected results H h HHHHH hHhhh GENETIC DISORDERS - Describe the condition of hemophilia. Male with hemophilia 3. Circle the Punnett squares that show individuals with hemophilia. X X WWWWW a Xa a X X XXXXX XX aXaX XXXXX XX X.X.XXXXX a XoXo C a Normal, heterozygous fernale XXXXX M aaa X X XXX

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,...

See similar textbooks

Similar questions

State whether each of the following genetic defects is inherited as an autosomal recessive, autosomal dominant, or X-linked recessive trait: phenylketonuria (PKU), sickle cell anemia, cystic fibrosis, Tay-Sachs disease, Huntingtons disease, and hemophilia A.
Could an individual with blood type O (genotype ii) be a legitimate child of parents in which one parent had blood type A and the other parent had blood type B?
The genotype XXY corresponds to Klinefelter syndrome Turner syndrome Triplo-X Jacob syndrome
Achondroplasia is a rare dominant autosomal defect resulting in dwarfism. The unaffected brother of an individual with achondroplasia is seeking counsel on the likelihood of his being a carrier of the mutant allele. What is the probability that the unaffected client is carrying the achondroplasia allele?
Classical hemophilia is a sex-linked disease caused by a recessive gene on the X chromosome. (Hemophilia refers to diseases that cause delays in blood clotting.) If a woman who is acarrierof classical hemophilia has children with a normal male, give the ratios of the possible offspring with respect to classical hemophilia. Be sure to state both the genotypes and the phenotypes of each offspring. For genotypes, use X for a normal X chromosome, Xh for an X chromosome with the hemophilia gene, and Y for a normal Y chromosome. For phenotypes, if the offspring is female, be sure to state if homozygous normal, a carrier, or has the disease. If the offspring is a male, be sure to state if normal or has the disease.
Huntington’s disease, is an incurable neurodegenerative genetic disorder that affectsmuscle coordination and some cognitive functions, typically becoming noticeable inmiddle age. It results from an autosomal dominant gene (H) and there are no carriers ofthe disease. Two parents with Huntington’s disease have an affected child. What is theprobability that their next child will be an unaffected girl if they are not double-dominant?
Ch. 14-2 G6PD deficiency is an X-linked recessive disorder. When people who have this disorder eat fava beans, they have a dangerous acute reaction in which a large number of their red blood cells rupture. A mother has the disorder; the father does not. What is the chance that any child of this union will have the trait?
1. Hemophilia is due to a sex-linked gene. It is recessive and found on the X chromosome. A woman who is a carrier for hemophilia marries a normal man. What will be the possible phenotypes of their children? Use a punnet square. 2. A phenotypically normal man, who has a hemophiliac brother, marries a normal woman, who is not a carrier. What is the probability that any of their children will be hemophiliac? Use a punnet square. 3. Color-blindness is an X-linked, recessive trait. If a normal-sighted woman, whose father was color-blind, marries a colorblind man, what is the probability that they will have a son who is color-blind? Use a punnet square. 4. A man and woman, both of normal vision, have: 1) a color-blind son (#1) who has a daughter of normal vision 2) a daughter (#1) of normal vision who has one color-blind son and one normal vision son 3) another daughter (#2) of normal vision who has five sons, all with normal vision What are the probable genotypes of the…
Shown above is a family pedigree tree in which family members afflictedwith the disease Haemophilia are shown with filled-in squares (male) or circles (females). A couple is trying to determine the likelihood of passingon the disease to their future children (represented by the ? symbolabove) because the hemophilia runs in the woman’s family. Turner syndrome is a disease in which an individual is bornwith only a single X chromosome. Suppose the woman in thecouple is a carrier for hemophilia and has a child with Turnersyndrome. Would this child have the disease?
Neurofibromatosis-1 (NF1) is an autosomal dominant disorder where tumours form in the base layer of the skin or in nerve tissues. What is the probability that individuals II-1 and II-2 will have a genetic son with NF1? Find the image attached.
Hemophilia A is transmitted by an X-linked recessive gene.With an affected father, what is the probability that a childwill have the disease? With an affected father and a carriermother, what is the probability?
A woman who sought genetic counseling is found to be heterozygousfor a chromosomal rearrangement between the second andthird chromosomes. Her chromosomes, compared to those in anormal karyotype, are diagrammed on the next page:(a) What kind of chromosomal aberration is shown?