Published in Am J Hum Genet on March 01, 1997
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Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats. Mol Cell (1999) 1.83
Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndrome. Hum Mol Genet (2000) 1.76
Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region. Hum Mol Genet (1995) 1.75
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Characterization of the nucleolar gene product, treacle, in Treacher Collins syndrome. Mol Biol Cell (2000) 1.38
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Mutations in the Treacher Collins syndrome gene lead to mislocalization of the nucleolar protein treacle. Hum Mol Genet (1998) 1.13
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