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The difference between them is that :

In genomic imprinting : one of the alleles in the two chromosomes ( for example the color of the eyes ) are tend to be heavily methylated, in contrast to the nonimpringting copy of the allele which typically is not methylated.

In X-chromosome in activation : As you know in female there are two X chromosomes, so one of the two X xhromosomes is methylated which mean one of the two chromosomes become inactivation.

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Q: What is the difference between x-inactivation and genomic imprinting?
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What phenomenon occurs when a particular alelle will either be expressed or silenced depending on whether it is inherited from a male or female?

genomic imprinting is the answer to the question above....found in my text book...


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Related questions

What has the author Eric Engel written?

Eric Engel has written: 'Genomic imprinting and uniparental disomy in medicine' -- subject(s): Chromosome abnormalities, Genetic disorders, Genomic imprinting


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A widely accepted hypothesis for the evolution of genomic imprinting is the "parental conflic.


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T or F Genomic imprinting and genetic anticipation both involve the inhibition of specific genes or chromosomes based on parental origin?

Are you from FAU Schwartz? Cuz I was looking up the same question.


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