Developmental Biology of Uterine Glands von GRAY, C. Allison, BARTOL, Frank F, TARLETON, Becky J, WILEY, Anne A, JOHNSON, Greg A, BAZER, Fuller W, SPENCER, Thomas E

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Characterization of the full fragile X syndrome mutation in fetal gametes von Malter, Henry E, Iber, Jane C, Willemsen, R, Graaff, Esther de, Tarleton, Jack C, Leisti, J, Warren, Stephen T, Oostra, Ben A

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Cognitive effects of diarrhea, malnutrition, and Entamoeba histolytica infection on school age children in Dhaka, Bangladesh von TARLETON, Jessica L, HAQUE, Rashidul, MONDAL, Dinesh, JIANFEN SHU, FARR, Barry M, PETRI, William A

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Estrogen-induced disruption of neonatal porcine uterine development alters adult uterine function von Tarleton, B.J, Braden, T.D, Wiley, A.A, Bartol, F.F

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Ovary-independent estrogen receptor expression in neonatal porcine endometrium von Tarleton, B.J, Wiley, A.A, Spencer, T.E, Moss, A.G, Bartol, F.F

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A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases von Rousseau, F, Heitz, D, Tarleton, J, MacPherson, J, Malmgren, H, Dahl, N, Barnicoat, A, Mathew, C, Mornet, E, Tejada, I

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Endometrial development and adenogenesis in the neonatal pig: effects of estradiol valerate and the antiestrogen ICI 182,780 von Tarleton, B.J, Wiley, A.A, Bartol, F.F

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Expression and Molecular Characterization of Estrogen Receptor Alpha Messenger RNA in Male Reproductive Organs of Adult Goats von MANSOUR, Mahmound M, MACHEN, Margo R, TARLETON, Becky J, WILEY, Anne A, WOWER, Jacek, BARTOL, Frank F, GOYAL, Hari O

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Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome von MCCONKIE-ROSELL, A, LACHIEWICZ, A. M, SPIRIDIGLIOZZI, G. A, TARLETON, J, SCHOENWALD, S, PHELAN, M. C, PONMANI GOONEWARDENA, XIAOHUA DING, BROWN, W. T

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Evidence of founder chromosomes in fragile X syndrome von Richards, R.I., Holman, K., Friend, K., Kremer, E., Hillen, D., Staples, A., Brown, W.T., Goonewardena, P., Tarleton, J., Schwartz, C., Sutherland, G.R.

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Keratinocyte growth factor expression by the bovine corpus luteum von Salli, U. (Oregon State University, Corvallis, OR.), Bartol, F.F, Wiley, A.A, Tarleton, B.J, Braden, T.D

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Regulation of Caulobacter crescentus ilvBN gene expression von TARLETON, J. C, MALAKOOTI, J, ELY, B

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Neonatal estradiol exposure alters uterine morphology and endometrial transcriptional activity in prepubertal gilts von Tarleton, Becky J., Wiley, Anne A., Bartol, Frank F.

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An Extensive de novo deletion removing FMR1 in a patient with mental retardation and the fragile X syndrome phenotype von Tarleton, Jack, Richle, Renee, Schwarsz, Charles, Rao, Kathleen, Aylsworth, Arthur S., Lachlewicz, Ave

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Molecular genetic advances in fragile X syndrome von TARLETON, J. C, SAUL, R. A

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Evidence of founder chromosomes in fragile X syndrome von Goonewardena, P, Schwartz, C, Sutherland, G.R, Tarleton, J, Holman, K, Hillen, D, Staples, A, Friend, K, Kremer, E, Richards, R.I, Brown, W.T

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Expression and Molecular Characterization of Estrogen Receptor Alpha Messenger RNA in Male Reproductive Organs of Adult Goats1 von Mansour, Mahmoud M, Machen, Margo R, Tarleton, Becky J, Wiley, Anne A, Wower, Jacek, Bartol, Frank F, Goyal, Hari O

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Molecular heterogeneity of the fragile X syndrome von NAKAHORI, Y, KNIGHT, S. J. L, DAVIES, K. E, HIRST, M. C, HOLLAND, J, SCHWARTZ, C, ROCHE, A, TARLETON, J, WONG, S, FLINT, T. J, FROSTER-ISKENIUS, U, BENTLEY, D

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Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy von SCHWARTZ, L. S, TARLETON, J, POPOVICH, B, SELTZER, W. K, HOFFMAN, E. P

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Isolation and characterization of ilvA, ilvBN, and ilvD mutants of Caulobacter crescentus von TARLETON, J. C, ELY, B

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