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alleles (1) 1
allelomorphism (1) 1
ataxia (1) 1
cgg expansions (1) 1
common (1) 1
etiology (1) 1
fmr1 (1) 1
fmr1 intermediate alleles (1) 1
fmr1 protein (1) 1
fragile x mental retardation protein (1) 1
fragile x syndrome (1) 1
gene (1) 1
genetic counseling (1) 1
genetics & heredity (1) 1
gray zone (1) 1
gray-zone (1) 1
intermediate alleles (1) 1
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movement disorders (1) 1
mutations (1) 1
neurodevelopmental disorders (1) 1
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population genetics (1) 1
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primary ovarian insufficiency (1) 1
range (1) 1
repeat expansion (1) 1
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women (1) 1
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