BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
10th Edition
ISBN: 9781305967359
Author: STARR
Publisher: CENGAGE L
expand_more
expand_more
format_list_bulleted
Concept explainers
Textbook Question
Chapter 14, Problem 14SA
Klinefelter syndrome (XXY) can be easily diagnosed by _______ .
a. pedigree analysis | c. karyotyping |
b. aneuploidy | d. |
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
Klinefelter syndrome (XXY) can most be easily diagnosed by_______ . a. pedigree analysis c. karyotyping b. aneuploidy d. phenotypic treatment
Color blindness is inherited in a(n)_____ pattern. a. autosomal dominant c. X-linked dominant b. autosomal recessive d. X-linked recessive
which is male with small testes, enlarged breasts,
The genotype XXY corresponds to
and decrease in body hair.
a. Turner syndrome
O b. Triplo-X
Oc. Klinefelter syndrome
d. Jacob syndrome
Chapter 14 Solutions
BIOLOGY:CONCEPTS+APPL.(LOOSELEAF)
Ch. 14 - Constructing a family pedigree is particularly...Ch. 14 - Prob. 2SACh. 14 - Prob. 3SACh. 14 - Prob. 4SACh. 14 - Prob. 5SACh. 14 - A trait that is present in a male child but not in...Ch. 14 - Color blindness is a case of ________ inheritance....Ch. 14 - Prob. 8SACh. 14 - Alleles for Tay-Sachs disease are inherited in an...Ch. 14 - Prob. 10SA
Ch. 14 - Prob. 11SACh. 14 - Prob. 12SACh. 14 - Prob. 13SACh. 14 - Klinefelter syndrome XXY can be easily diagnosed...Ch. 14 - Match the chromosome terms appropriately. ___...Ch. 14 - Does the phenotype indicated by the red circles...Ch. 14 - Human females have two X chromosomes XX; males...Ch. 14 - Somatic cells of individuals with Down syndrome...Ch. 14 - An allele responsible for Marfan syndrome Section...Ch. 14 - Both Duchenne muscular dystrophy and color...
Knowledge Booster
Learn more about
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
- Colorblindness is a recessive x-linked trait. Which genotype represents a male with normal vision? a. XNXN b. XYN c. XnY d. XNYarrow_forwardThis example can be considered as ______________. A.Modifier gene B.Gene redundancy C.Co-dominance D.Incomplete dominancearrow_forwardColor blindness is an x-linked recessive disorder. A woman who is a carrier for color blindness has children with a man who is color blind. Determine the probability that their child will be color blind. a. 0 % b. 25% c. 50% d. 100%arrow_forward
- von Gierke's disease is inherited as A. Autosomal dominant B. Autosomal recessive C. X-linked recessive D. X-linked dominantarrow_forwardA trait that is present in a male child but not in either of his parents is characteristic of inheritance. a. autosomal dominant b. autosomal recessive c. X-linked recessive d. It is impossible to answer this question without more informationarrow_forwardWhen we say that a woman is a carrier for a genetic disease or disorder it means that a. she can pass the gene only to male children b. she has 1 gene, but not the disorder c. she can pass the gene only to female children d. she has 2 genes for the disorderarrow_forward
- A disorder that only ever appears in males and is present in all male children is a(n) ________. a. Y-linked disorder b. autosomal dominant disorder c. X-linked dominant disorderarrow_forwardA boy is color-blind (X-linked recessive) and has a straight hairline (autosomal recessive). Which could be the genotype of his mother? Select one: А. Вbxwxw B. Bbww C. Xbxbww D. Xbywwarrow_forwardIdentify genetic terms and basic principles of genetics as applied to blood groups, sex-linkage, and other inherited characteristics. a. Genetics b. Inheritance theory c. Sex-linked characteristics d. Linkagearrow_forward
- Color blindness is a case of ________ inheritance. a. autosomal dominant c. X-linked dominant b. autosomal recessive d. X-linked recessivearrow_forwardPolydactyly is a congenital physical anomaly in in humans, dogs, cats; and having supernumerary fingers or toes. If it is an autosomal dominant trait, when is a genotype of a person that shows normal phenotype? a. heterozygous recessive b. heterozygous dominant c. homozygous recessive d. homozygous dominantarrow_forwardConsanguinity is having offspring together who are blood-related. Their children have a higher risk of having a second child with an autosomal recessive condition A. Both statements are correct B. Both statements are incorrect C. Statement 1 is correct. Statement 2 is incorrect D. Statement 2 is correct. Statement 1 is incorrectarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
How to solve genetics probability problems; Author: Shomu's Biology;https://www.youtube.com/watch?v=R0yjfb1ooUs;License: Standard YouTube License, CC-BY
Beyond Mendelian Genetics: Complex Patterns of Inheritance; Author: Professor Dave Explains;https://www.youtube.com/watch?v=-EmvmBuK-B8;License: Standard YouTube License, CC-BY