A human dopamine transporter cDNA predicts reduced glycosylation, displays a novel repetitive element and provides racially-dimorphic TaqI RFLPs

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A comprehensive set of sequence analysis programs for the VAX

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Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member

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Dopamine Transporters, Substance Abuse, Psychoactive Drug +14

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

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