BIOLOGY
4th Edition
ISBN: 9781266739606
Author: Hoefnagels
Publisher: MCG
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Textbook Question
Chapter 35, Problem 10MCQ
A chemical that can cause a birth defect is a
a. toxin.
b. trisomy.
c. mutagen.
d. teratogen.
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Chapter 35 Solutions
BIOLOGY
Ch. 35.1 - Prob. 1MCCh. 35.1 - Prob. 2MCCh. 35.1 - Prob. 3MCCh. 35.2 - Prob. 1MCCh. 35.2 - Prob. 2MCCh. 35.2 - Prob. 3MCCh. 35.2 - Prob. 4MCCh. 35.3 - Prob. 1MCCh. 35.3 - Prob. 2MCCh. 35.3 - How do hormones regulate the ovarian and menstrual...
Ch. 35.4 - Prob. 1MCCh. 35.4 - Prob. 2MCCh. 35.4 - Prob. 3MCCh. 35.5 - What are the events of fertilization?Ch. 35.5 - What are the relationships among the zygote,...Ch. 35.5 - What is implantation, and when does it occur?Ch. 35.5 - Prob. 4MCCh. 35.5 - Prob. 5MCCh. 35.5 - What are the events of the second and third...Ch. 35.5 - Prob. 7MCCh. 35.6 - Prob. 1MCCh. 35.6 - Prob. 2MCCh. 35.6 - Prob. 3MCCh. 35.7 - Prob. 1MCCh. 35.7 - Prob. 2MCCh. 35 - Prob. 1MCQCh. 35 - Which hormones play central roles in both male and...Ch. 35 - Prob. 3MCQCh. 35 - Why can't a fertilized polar body develop into a...Ch. 35 - Prob. 5MCQCh. 35 - Prob. 6MCQCh. 35 - What is the correct order of structures to develop...Ch. 35 - Prob. 8MCQCh. 35 - A baby born four weeks before its due date is most...Ch. 35 - A chemical that can cause a birth defect is a a....Ch. 35 - What is differentiation? How do protein gradients...Ch. 35 - Prob. 2WIOCh. 35 - Prob. 3WIOCh. 35 - Prob. 4WIOCh. 35 - What are the functions of LH and FSH in males and...Ch. 35 - Prob. 6WIOCh. 35 - Prob. 7WIOCh. 35 - Prob. 8WIOCh. 35 - Is each of the following cell types haploid or...Ch. 35 - Prob. 10WIOCh. 35 - Prob. 11WIOCh. 35 - What would happen if two sperm fertilized the same...Ch. 35 - Prob. 13WIOCh. 35 - Prob. 14WIOCh. 35 - Prob. 15WIOCh. 35 - Prob. 16WIOCh. 35 - Prob. 17WIOCh. 35 - Prob. 18WIOCh. 35 - Prob. 19WIOCh. 35 - Most physicians clamp and cut the umbilical cord...Ch. 35 - Prob. 21WIOCh. 35 - Prob. 22WIOCh. 35 - What kinds of studies and information would be...Ch. 35 - Review the Survey the Landscape figure in the...Ch. 35 - Add ovulation to the concept map. What hormonal...Ch. 35 - Prob. 3PITCh. 35 - Add the terms placenta, follicle, polar body,...
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- In humans, hemophilia is an X-linked recessive condition characterized by the inability of blood to clot normally. A woman who is a carrier for hemophilia marries a man who has hemophilia. What are the genotypes of the woman and man, respectively? a. xH+xH+, xH+y b. xH+xH xH+y c. xH+xH xHy Od. XHXH, XH+y O e. xHxH xHyarrow_forwardMales can be said to be ‘weaker’ genetically because they are predisposed to disorders that are a result of sexually linked transmission. This is mainly because their genotype for ‘male’ is “spelled” as: A. XX B. DNA C. XY D. BBarrow_forwardJoe has classic hemophilia, an X-linked recessive disease. Could Joe have inherited the gene for this disease from the following people? Yes No a. His mother's mother b. His mother's father c. His father's mother d. His father's fatherarrow_forward
- von Gierke's disease is inherited as A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. X-linked dominantarrow_forwardIn order for a male to inherit a sex-linked (X-linked) disorder, he must receive the allele from: a. his mother only. b. either his mother or father. c. his father only. d. both his mother and father.arrow_forwardOne of the forms of rickets is inherited in the autosomal dominant way. This disease is a result of: Select one: a. Aneuploidy. O b. Changes in the number of chromosomes. c. Chromosomal mutations. e. Gene mutations. O d. Polyploidy.arrow_forward
- Hemophilia in humans is due to a mutation on the X chromosome. What will be the result of mating between a normal (non-carrier) female and a hemophiliac male? A. Half of the daughters are normal and half of the sons are hemophiliacs. B. All sons are normal and all daughters are carriers. C. All daughters are normal and all sons are carriers. D. Half of the children are normal and the other half are hemophiliacs; All daughters are carriers.arrow_forward------ is the transmission of DNA to offspring. a. Reproduction b.Development c. Homeostasis d. Inheritancearrow_forwardAn individual who is a carrier for a sex-linked trait such as hemophilia Select one: A. is always female. B. is homozygous for the recessive condition. C. cannot pass the gene on to his or her daughters. D. shows the dominant phenotype.arrow_forward
- A young man went to the doctor because he had small testes and enlarged breasts. Through chromosomal testing, it was determined that this young man had the sex chromosomes XXY. Identify the syndrome with which this young man was MOST likely diagnosed. A. Turner syndrome B. Klinefelter syndrome C. Cri du Chat syndrome D. Down syndromearrow_forwardHemophilia is a disease caused by a gene found on the X chromosome. Therefore, it is a sex-linked disease which is caused by the recessive allele. Suppose, a man with hemophilia marries a woman who is homozygous dominant for the trait. Predict the genotype of the man. (XH = normal; Xh= hemophiliac) * a. XH Y b. XHXh c. XhXh d. Xh Yarrow_forwardA 14-year-old girl has some abnormalities: her height is lower than that of the girls of the same age, the signs of puberty are absent, her neck is very short, her shoulders are wide. During the cytogenetic analysis the lack of one X-chromosome was found. The girl has normal intellectual development. What disease does the girl have? Select one: a. Turner's syndrome. b. Down's syndrome. c. Edward's syndrome. d. Patau syndrome. O e. Klinefelter's syndrome.arrow_forward
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