Emory University School of Medicine Warren Laboratory
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Publications - 1998

 

Gunter, C, Paradee, W, Crawford, DC, Meadows, KA, Newman, J, Kunst, CB, Nelson, DL, Schwartz, C, Murray, A, Macpherson, JN, Sherman, SL and Warren, ST: Reexamination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism of FMR1. Human Molecular Genetics 7:1935-1946 (1998). cover illustration.

Chou, H-H, Takematsu, H, Diaz, S, Iber, J, Nickerson, E, Wright, K, Muchmore, EA, Nelson, D, Warren, ST and Varki, A: A mutation in human CMP-sialic acid hydrolase occurred after Homo-Pan divergence. Proceedings of the National Academy of Sciences, USA 95:11751-11756 (1998).

Brown, V, Small, K, Lakkis, L, Feng, Y, Gunter, C, Wilkinson, KD and Warren, ST: Purified recombinant Fmrp exhibits selective RNA-binding as an intrinsic property of the fragile X mental retardation protein. Journal of Biological Chemistry 273:15521-15527 (1998).

Small, K and Warren, ST: Complete emerin deletions, resulting in Emery-Dreifuss muscular dystrophy, occurring on either Xq28 inversion backgrounds. Human Molecular Genetics 7:135-140 (1998).

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