Primary oocytes in females are O dipoid and undergo mitosis O dplcid and undergo meiosis O haploid and undergo mitosis haploid and undergo meiesis

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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**Question: Primary oocytes in females are:**

- ○ diploid and undergo mitosis
- ○ diploid and undergo meiosis
- ○ haploid and undergo mitosis
- ○ haploid and undergo meiosis
Transcribed Image Text:**Question: Primary oocytes in females are:** - ○ diploid and undergo mitosis - ○ diploid and undergo meiosis - ○ haploid and undergo mitosis - ○ haploid and undergo meiosis
**Question:**
Individuals with Klinefelter's syndrome have which of the following sex chromosome complements?

**Options:**
1. ◯ XYY
2. ◯ XX
3. ◯ XXX
4. ◯ XY
5. ◯ XO
6. ◯ XXY

**Explanation:**
This question is designed to test your knowledge of the chromosomal conditions associated with Klinefelter's syndrome. Klinefelter's syndrome is a genetic condition where males have an extra X chromosome. Therefore, individuals with this syndrome have the chromosomal complement XXY. 

**Correct Answer:** 
6. ◯ XXY

This information can be used to better understand the genetic causes and implications of various chromosomal arrangements and their associated syndromes.
Transcribed Image Text:**Question:** Individuals with Klinefelter's syndrome have which of the following sex chromosome complements? **Options:** 1. ◯ XYY 2. ◯ XX 3. ◯ XXX 4. ◯ XY 5. ◯ XO 6. ◯ XXY **Explanation:** This question is designed to test your knowledge of the chromosomal conditions associated with Klinefelter's syndrome. Klinefelter's syndrome is a genetic condition where males have an extra X chromosome. Therefore, individuals with this syndrome have the chromosomal complement XXY. **Correct Answer:** 6. ◯ XXY This information can be used to better understand the genetic causes and implications of various chromosomal arrangements and their associated syndromes.
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