What is your answer?
Which is NOT a guidline of the Research Group on Ethical, Social, and Legal Issues in Genetic Counseling and Genetic Engineering on genetic testing programs?
{ 1 } - People who have genetic defects should be advised not to procreate.
{ 2 } - Screening programs should be voluntary.
{ 3 } - Information about screening should be open and available to all.
{ 4 } - The information obtained should be made available according to clearly stated policies known to those participating before they consent, and their privacy should be carefully protected.
{ 5 } - Persons to be screened or who have their children screened should be informed before they consent about the nature and cost of therapy and its risks, or if no therapy is available.
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1 is correct!
Which is NOT a guidline of the Research Group on Ethical, Social, and Legal Issues in Genetic Counseling and Genetic Engineering on genetic testing programs?
{ 1 } - People who have genetic defects should be advised not to procreate.
{ 2 } - Screening programs should be voluntary.
{ 3 } - Information about screening should be open and available to all.
{ 4 } - The information obtained should be made available according to clearly stated policies known to those participating before they consent, and their privacy should be carefully protected.
{ 5 } - Persons to be screened or who have their children screened should be informed before they consent about the nature and cost of therapy and its risks, or if no therapy is available.
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Before continuing, you might try some wrong answers.
2 is wrong. Please try again.
Which is NOT a guidline of the Research Group on Ethical, Social, and Legal Issues in Genetic Counseling and Genetic Engineering on genetic testing programs?
{ 1 } - People who have genetic defects should be advised not to procreate.
{ 2 } - Screening programs should be voluntary.
{ 3 } - Information about screening should be open and available to all.
{ 4 } - The information obtained should be made available according to clearly stated policies known to those participating before they consent, and their privacy should be carefully protected.
{ 5 } - Persons to be screened or who have their children screened should be informed before they consent about the nature and cost of therapy and its risks, or if no therapy is available.
See p. 326.
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3 is wrong. Please try again.
Which is NOT a guidline of the Research Group on Ethical, Social, and Legal Issues in Genetic Counseling and Genetic Engineering on genetic testing programs?
{ 1 } - People who have genetic defects should be advised not to procreate.
{ 2 } - Screening programs should be voluntary.
{ 3 } - Information about screening should be open and available to all.
{ 4 } - The information obtained should be made available according to clearly stated policies known to those participating before they consent, and their privacy should be carefully protected.
{ 5 } - Persons to be screened or who have their children screened should be informed before they consent about the nature and cost of therapy and its risks, or if no therapy is available.
See p. 326.
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4 is wrong. Please try again.
Which is NOT a guidline of the Research Group on Ethical, Social, and Legal Issues in Genetic Counseling and Genetic Engineering on genetic testing programs?
{ 1 } - People who have genetic defects should be advised not to procreate.
{ 2 } - Screening programs should be voluntary.
{ 3 } - Information about screening should be open and available to all.
{ 4 } - The information obtained should be made available according to clearly stated policies known to those participating before they consent, and their privacy should be carefully protected.
{ 5 } - Persons to be screened or who have their children screened should be informed before they consent about the nature and cost of therapy and its risks, or if no therapy is available.
See p. 326.
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5 is wrong. Please try again.
Which is NOT a guidline of the Research Group on Ethical, Social, and Legal Issues in Genetic Counseling and Genetic Engineering on genetic testing programs?
{ 1 } - People who have genetic defects should be advised not to procreate.
{ 2 } - Screening programs should be voluntary.
{ 3 } - Information about screening should be open and available to all.
{ 4 } - The information obtained should be made available according to clearly stated policies known to those participating before they consent, and their privacy should be carefully protected.
{ 5 } - Persons to be screened or who have their children screened should be informed before they consent about the nature and cost of therapy and its risks, or if no therapy is available.
See p. 327.
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the end