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Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression
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Characterization of regions functional in the nuclear localization of the Fanconi anemia group A protein
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PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival
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A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators
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N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma
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Sialidase-mediated depletion of G~M~2 ganglioside in Tay - Sachs neuroglia cells
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T-STAR/ETOILE: a novel relative of SAM68 that interacts with an RNA-binding protein implicated in spermatogenesis
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Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)
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Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis
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Large genomic duplicons map to sites of instability in the Prader - Willi/Angelman syndrome chromosome region (15q11-q13)
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Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background
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