(x-linked genes q9)you don't have to answer question 8, please answer question 9 9. A woman who is a carrier marries a normal man. Show the cross. What is the probability thattheir children will have hemophilia? What sex will a child in the family with hemophilia be? In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Maleswill either have the disease or not (but they won't ever be carriers)HHX"x"x"Y= female, normalmale, normalX X = female, carrierx"x"X" Y= male, hemophiliacx" x"X" X= female, hemophiliac8. What is the probability that their children will have the disease?

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Description: (x-linked genes q9)you don't have to answer question 8, please answer question 9 9. A woman who is a carrier marries a normal man. Show the cross. What is the probability thattheir children will have hemophilia? What sex will a child in the family wi

Inheritance patterns are of different type’s Mendelian inheritance, incomplete dominance,…

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9. A woman who is a carrier marries a normal man. Show the cross. What is the probability that their children will have hemophilia? What sex will a child in the family with hemophilia be?

Basic Clinical Laboratory Techniques 6E

6th Edition

ISBN:9781133893943

Author:ESTRIDGE

Publisher:ESTRIDGE

Chapter2: Basic Hematology

Section2.1: Introduction To Hematology

Problem 14RQ

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1. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Males will have the disease or not (but they won't be ever carriers) XH XH = female, normal XH Xh = female, carrier Xh Xh = female, hemophilic XH Y = male, normal Xh Y = male, hemophilic a) Show the cross of a man who has hemophilia with a woman who is a carrier. b) What is the probability that their children have the disease
Normal No Spac Hemophilia is a blood clotting disorder that almost exclusively affects males. It is a sex-linked, recessive disorder (X). Using the details below, fill in the Punnett square to determine the percent probability of the couple having a child with hemophilia. Mother Father -carrier of -does not have hemophilia hemophilia -genotype XHX -genotype XY Mother. XH. Xh Father Probability of offspring having hemophilia: OFocus
3. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Males will either have the disease or not (but they won't ever be carriers). Show the cross of a man who has hemophilia with a woman who is a carrier. XH XH = female, normal XH Xh= female, carrier xh Xh= female, hemophiliac XH Y = male, normal Xh Y= male, hemophiliac 4. What is the probability that their children will have the disease? 5. A woman who is a carrier "marries" a normal man. Show the cross. What is the probability that their children will have hemophilia? What sex will a child in the family with hemophilia be? 6. In a certain cactus, prickly spines can be two pronged or one pronged. If a true breeding one- pronged cactus is crossed with a true breeding two-pronged cactus, the F1 generation has a mixture of spines, some are two-pronged, some are one-pronged. a. Is this an example of codominance or incomplete dominance? b. Show the F2 generation (a cross between the two…
A father without hemophilia (X HY) has two daughters and two sons. Neither daughter has hemophilia. One son has hemophilia and the other does not. What is the genotype of the mother? O A XHXH O B. XHxh O c xhy O D. XHY acer
(x-linked genes q8) Please answer this question for me
I need this to be : to be shown as superscript on the X chromosomes
is thal ui ANensn 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 lertilizations Male children XhY Xhx XhY XhX Paternal gametes Paternal gametes Female children 00 00 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…
4. STATEMENT: A woman who has blood type B positive has a daughter who is type 0 positive and a son who is type A negative. a) What is the genotype for the woman, daughter, son and man? Woman Daughter Son Man Genotype b) The woman and the man surprising are having a third child. What are the possible genotypes and phenotypes for their third child?
2. STATEMENT: A woman and man both do not have sickle-cell anemia, but both had one parent who had sickle cell. Sickle-cell is an autosomal (somatic) recessive trait. a) What is the genotype for the woman, man and each of their parents? b) This couple unexpectedly is going to have their first child. i. What's the probability that their child will have not have sickle cell like the couple? ii. What's the probability that the child will have sickle cell like one the grandparents?
In humans, as well as with many other animals, sex is determined by special sex chromosomes. An individual containing two X chromosomes is a female, while an individual possessing an X and Y chromosome is a male. he sex chromosomes bear alleles for traits. Sex linkage applies to genes that are located on the sex chromosomes. These genes are considered sex-linked because their expression and inheritance patterns differ between males and females. The genes present on the X chromosome are said to be X linked. Many more genes are present on the X chromosome than found on the Y chromosome. Nonetheless, those genes found on the Y chromosome are said to be Y linked. The Y chromosome is smaller than its homologue, the X chromosome. Consequently, most of the loci present on the X chromosome are absent on the Y chromosome. 1. In humans, hemophilia is a sex linked trait. Females can be normal, carriers, or have the disease. Males will have the disease or not (but they won't be ever carriers) XH…
Is the trait correct?
Affected female Affected male O Unaffected female Unaffected male 11 IV ||| O 40/20 20 80/40 80 OOT 180 90/20 160/20 20 A) Between 20 and 40 and between 80 and 180, respectively B) Between 20 and 40 and between 160 and 180, respectively C) Between 40 to 80 and between 160 and 180, respectively D) Between 40 to 80 and between 180 and 200, respectively O 40/20 80/20 160 Wint Matty Mariant 20 180/20 20 180/40 20 180/20 250/20 200 20/20 160/20 20 200 20 arches s 20/20 20 simp ww byern 118. A 25-year-old nulligravid woman (individual IV-1 in the pedigree shown) and her 28-year-old husband come to the office for counseling prior to conception. Previous reproductive endocrinologic evaluation of the husband showed no abnormalities. The woman has a family history of fragile X syndrome. The genotype of the CGG trinucleotide repeat length in the 5'-untranslated exon of the FMR1 gene for each individual in the family is indicated. Based on these findings, the repeat length boundaries between…