Which trinucleotide repeat sequence is expanded in the FMR1 gene in people with Fragile X Syndrome?
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Which trinucleotide repeat sequence is expanded in the FMR1 gene in people with Fragile X Syndrome?
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What is the consequence of the FMR1 gene mutation in Fragile X Syndrome?
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The only way to be sure is through a simple blood test called the FMR1 test.
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The only way to be sure is through a simple blood test called the FMR1 test.
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Which population is most likely to be carriers of Fragile X Syndrome?
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20% of Women Carriers of the Fragile X Premutation Face Fertility Issues: This is The Hidden Impact of the FMR1 Premutation. This powerful discussion brings to light the wide-ranging effects of the FMR1 premutation, For carriers of the FMR1 gene, the effects can include a high rate of reproductive issues, specifically fertility problems affecting about one in five women carriers. This statistic, clearly outlined in the video, is a call to greater genetic awareness. When a woman is unaware of her
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Speed roasting KSI 🤣 Big forehead developmental delay in kids = which syndrome? ⸻ Explanation: \t•\tFragile X (correct): X-linked, CGG repeat on FMR1. Features: large forehead, long face, big ears, macroorchidism. Most common inherited cause of intellectual disability. \t•\tTurner (45,XO): short stature, webbed neck, streak ovaries. \t•\tDown (Trisomy 21): flat facies, single palmar crease, hypotonia, ID. \t•\tKlinefelter (47,XXY): tall males, small testes, gynecomastia, infertility. ⸻ Answer:
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