The objects shown above are in the scratch area of the publication.
Definitions:
Fragile X Syndrome
A human genetic disorder caused by a fragile site that occurs near the tip on the X chromosome; effects range from mild learning disabilities to severe intellectual disability and hyperactivity.
CGG Sequences
Specific sequences of DNA nucleotides comprising cytosine and guanine, often studied for their role in genetic diseases.
Genomic Imprinting
A biological occurrence where specific genes are manifested based on which parent they are inherited from.
Polyploidy
The condition of having more than two complete sets of chromosomes, common in plants and some animal species.
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