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Author Question: Prader-Willi syndrome is a genetic disorder involving a partial deletion of chromosome 15q on the ... (Read 72 times)

SAVANNAHHOOPER23

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on: Jan 12, 2022
Prader-Willi syndrome is a genetic disorder involving a partial deletion of chromosome 15q on the paternal chromosome. When both copies of a gene (or chromosome) are functional but only one is expressed, this is an example of ________.
◦ position effect variegation
◦ X-inactivation
◦ genomic imprinting
◦ histone acetylation
◦ chromatin modifications
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Marked as best answer by SAVANNAHHOOPER23 on Jan 12, 2022

soda0602

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Reply #1 on: Jan 12, 2022
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SAVANNAHHOOPER23

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Reply 2 on: Jan 12, 2022
Thanks for the timely response, appreciate it

essyface1

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Reply 3 on: Yesterday
Great answer, keep it coming :)

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