Warren Laboratory

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Publications 1997     Eberhart, DE and Warren, ST: The molecular basis of fragile X syndrome. Cold Spring Harbor Symposium on Quantitative Biology: Function and Dysfunction in the Nervous System. 61:679-687 (1997). Feng, Y, Absher, D, Eberhart, DE, Brown, V, Malter, HE and Warren, ST: FMRP associates with polyribosomes as an mRNP and the I304N mutation of severe fragile X syndrome abolishes this association. Molecular Cell 1:109-118 (1997). Kenneson, A, Cramer, DW and Warren, ST: Fragile X premutations are not a major cause of early menopause. American Journal of Human Genetics 61:1362-1369 (1997). Losekoot, M, Hoogendoorn, E, Olmar, R, Jansen, CCAM, Oosterwolk, JC, van den Ouweland, AMW, Halley, DJJ, Warren , ST, Willemsen, R, Oostra, BA and Bakker, E: Prenatal diagnosis for the fragile X syndrome: Loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. Journal of Medical Genetics 34:924-926 (1997). Kunst, CB, Leeflang, EP, Iber, JC, Arnheim, N and Warren, ST: The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing. Journal of Medical Genetics 34:627-631 (1997). Small, K, Iber, J and Warren, ST: Emerin deletion reveals a common X-chromosome nversion mediated by inverted repeats. Nature Genetics 16:96-99 (1997). Small, K, Wagener, M and Warren, ST: Isolation and characterization of the complete mouse emerin gene. Mammalian Genome 8:337-341 (1997). Warren, ST: Trinucleotide repetition and fragile X syndrome. Hospital Practice 32:73 - 98 (1997). cover illustration. Feng, Y, Gutekunst, C-A, Eberhart, DE, Yi, H, Warren, ST and Hersch, SM: Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodentritic ribosomes. Journal of Neuroscience 17:1539-1547 (1997). Malter, H, Iber, JC, Willemsen, R, de Graaff, E, Tarleton, JC, Leisti, J, Warren, ST and Oostra, BA: Characterization of the full fragile X syndrome mutation in fetal gametes. Nature Genetics 15:165-169 (1997). Warren, ST: Polyalanine expansion in synpolydactaly might result from unequal crossing-over of HOXD13. Science 275:408-409 (1997).

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