4.2 Review

The FRAXopathies: Definition, Overview, and Update

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Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles

SL Nolin et al.

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Transport of fragile X mental retardation protein via granules in neurites of PC12 cells

YD Otero et al.

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Slipped-strand DNAs formed by long (CAG).(CTG) repeats: slipped-out repeats and slip-out junctions

CE Pearson et al.

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A Mankodi et al.

CURRENT OPINION IN NEUROLOGY (2002)

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Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile X syndrome

B Coffee et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2002)

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Timing of the absence of FMR1 expression in full mutation chorionic villi

R Willemsen et al.

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Altered synaptic plasticity in a mouse model of fragile X mental retardation

KM Huber et al.

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CJM Bontekoe et al.

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Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel

H Toledano-Alhadef et al.

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The fragile X mental retardation protein inhibits translation via interacting with mRNA

ZZ Li et al.

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J Mallolas et al.

MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY (2001)

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Evidence that fragile X mental retardation protein is a negative regulator of translation

B Laggerbauer et al.

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No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers

A Murray et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)

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Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations

RDL Hundscheid et al.

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