Fragile X syndrome - disorder in humans caused by the inheritance of genes that have undergone insertions of a string of 3 or 4 nucleotides, repeated over and over.

TRUE

FALSE

Question

Dylan Reed

Biology

5 December, 05:41

Fragile X syndrome - disorder in humans caused by the inheritance of genes that have undergone insertions of a string of 3 or 4 nucleotides, repeated over and over.

TRUE

FALSE

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Answers (1)

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Harper Fry · Answer 1

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Explanation:

Fragile X syndrome is a disorder in which nucleotide repeats will result in increase in copy number which will make the threshold unstable < it is basically a trinucleotide repeat disorder

Fragile X syndrome - disorder in humans caused by the inheritance of genes that have undergone insertions of a string of 3 or 4 nucleotides, repeated over and over.TRUEFALSE

Fragile X syndrome - disorder in humans caused by the inheritance of genes that have undergone insertions of a string of 3 or 4 nucleotides, repeated over and over.

TRUE

FALSE