Published in Lancet on March 23, 1985
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A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16. Nature (1985) 7.34
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Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nat Genet (1992) 5.12
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Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. J Biol Chem (1990) 3.87
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin. Nature (1990) 3.84
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. Am J Hum Genet (1985) 3.83
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Distinct actions of cis and trans ATP within the double ring of the chaperonin GroEL. Nature (1997) 3.48
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The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif. EMBO J (2001) 3.42
Cloning of human androgen receptor complementary DNA and localization to the X chromosome. Science (1988) 3.40
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Immunoelectron microscopic localization of dystrophin in myofibres. Nature (1988) 3.37
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