Biology: Concepts and Investigations
5th Edition
ISBN: 9781260259049
Author: Hoefnagels
Publisher: MCG
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Textbook Question
Chapter 35, Problem 8MCQ
A chemical that can cause a birth defect is a
a. toxin.
b. trisomy.
c. mutagen.
d. teratogen.
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A female born with Angelman syndrome carries a deletion in theAS gene (i.e., the UBE3A gene). Which parent transmitted thedeletion to her?a. Her father c. Either her mother or fatherb. Her mother
Males 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.
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B.
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XY
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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.
Chapter 35 Solutions
Biology: Concepts and Investigations
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 - A chemical that can cause a birth defect is a a....Ch. 35 - Prob. 1WIOCh. 35 - Prob. 2WIOCh. 35 - Prob. 3WIOCh. 35 - Prob. 4WIOCh. 35 - Prob. 5WIOCh. 35 - Prob. 6WIOCh. 35 - Is each of the following cell types haploid or...Ch. 35 - Prob. 8WIOCh. 35 - Prob. 9WIOCh. 35 - What would happen if two sperm fertilized the same...Ch. 35 - Prob. 11WIOCh. 35 - Prob. 12WIOCh. 35 - Prob. 13WIOCh. 35 - Prob. 14WIOCh. 35 - Prob. 15WIOCh. 35 - Prob. 16WIOCh. 35 - Prob. 17WIOCh. 35 - Prob. 18WIOCh. 35 - Prob. 19WIOCh. 35 - Review the Survey the Landscape figure in the...Ch. 35 - Add ovulation to the concept map. What hormonal...Ch. 35 - Add the terms placenta, follicle, polar body,...
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- One 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_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_forwardAn individual has the chromosomal makeup XX and sexual differentiation proceeds normally. Which of the following would be the case? a. Mullerian ducts will degenerate b. Estrogen promotes development of the vagina c. Anti-Mullerian hormone is present d. Wolffian ducts will develop e. There will be no formation of fetal testesarrow_forward
- The marking process for genomic imprinting initially occursduringa. gametogenesis. c. embryonic development.b. fertilization. d. adulthoodarrow_forwardWhen the phenotype of the offspring is determined by endoparasites in the father it is… a. epistasis b. due to genes located in the mitochondria. c. a maternal effect d. non-nuclear inheritance e. a non-additive genetic effectarrow_forwardVirtually all steps of embryological development depend on: a. Alterations in the genome b. Tumor Stem Cells c. Changes in programs of gene expression d. Telomerasearrow_forward
- Which of the following statements is/are true? A. Spermatogenesis is an example of asymmetric cell division. B. The formation of a mature egg occurs through symmetric cell division. C. Spermatogenesis and oogenesis are both examples of asymmetric cell division. D. Spermatogenesis involves only symmetric cell division whereas oogenesis involves asymmetric cell division.arrow_forwardIt is estimated that in about 1/150,000 births, an individual is born with 46 chromosomes, both an X and a Y chromosome, but is externally a phenotypic female at birth. A mutation in the gene for which protein is the most likely explanation for this condition? A. Chorionic gonadotropin B. Anti-Müllerian hormone receptor C. Testes determining factor D. Wolffian regression factor (WRF) E. Estrogen receptor βarrow_forwardPlease choose the correct answer. If a recessive mutation kills an individual during the early stages of its development, what is the possible mode of inheritance exhibited if a recessive F1 with heterozygous parents survives? a. epigenetic inheritance b. maternal inheritance c. maternal effect d. organelle inheritancearrow_forward
- a. The ovaries produce secondary the female sex cells. b. Stem cells, called divide by to produce primary each form part of a c. At the onset of puberty, tens of thousands of ovaries. Between menarche and menopause, each primordial follicle develops into a in the and its primary oocyte completes d. Some primary oocytes become 23-chromosome cells that begin then pause. secondary oocyte is released into is completed when e. Each month, the uterine tube. the oocyte isarrow_forwardAt fertilization, a sperm contributes a. a diploid nucleus. b. mRNAs. c. a centrosome. d. nutrients.arrow_forwardIn genetic maternal effect, the phenotype of the individual is determined by which of these statements? A. The sex of the parent who transmits the gene B. The nuclear genotype of the maternal parent C. The sex of the individual with only one sex able to express the phenotype D. Cytoplasmic genes usually located in the mitochondria E. A combination of environmental factors and the genotype of the individualarrow_forward
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Mitochondrial mutations; Author: Useful Genetics;https://www.youtube.com/watch?v=GvgXe-3RJeU;License: CC-BY