Isolation and characterization of ilvA, ilvBN, and ilvD mutants of Caulobacter crescentus.

Por Tarleton, J C, Ely, B
Publicado em 1991

Direct analysis of the FMR-1 gene provides an explanation for an exceptional case of a fragile X negative, mentally retarded male in a fragile X family.

Por Tarleton, J, Wong, S, Schwartz, C
Publicado em 1992

The use of a new multiplex PCR assay significantly improves the rapid detection of deletions in the dystrophin gene.

Por Tarleton, J C, Schwartz, C E
Publicado em 1991

Regulation of Caulobacter crescentus ilvBN gene expression.

Por Tarleton, J C, Malakooti, J, Ely, B
Publicado em 1994

Difficult diagnosis of the fragile X syndrome made possible by direct detection of DNA mutations.

Por Tarleton, J, Wong, S, Heitz, D, Schwartz, C
Publicado em 1992

Identification, distribution, and sequence analysis of new insertion elements in Caulobacter crescentus.

Por Ohta, N, Mullin, D A, Tarleton, J, Ely, B, Newton, A
Publicado em 1990

Fluorescent multiplex linkage analysis and carrier detection for Duchenne/Becker muscular dystrophy.

Por Schwartz, L S, Tarleton, J, Popovich, B, Seltzer, W K, Hoffman, E P
Publicado em 1992

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype

Por Tarleton, J, Kenneson, A, Taylor, A, Crandall, K, Fletcher, R, Casey, R, Hart, P, Hatton, D, Fisch, G, Warren, S
Publicado em 2002

Molecular heterogeneity of the fragile X syndrome.

Por Nakahori, Y, Knight, S J, Holland, J, Schwartz, C, Roche, A, Tarleton, J, Wong, S, Flint, T J, Froster-Iskenius, U, Bentley, D
Publicado em 1991

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

Por McConkie-Rosell, A, Lachiewicz, A M, Spiridigliozzi, G A, Tarleton, J, Schoenwald, S, Phelan, M C, Goonewardena, P, Ding, X, Brown, W T
Publicado em 1993

The elusive Angelman syndrome critical region.

Por Trent, R J, Sheffield, L J, Deng, Z M, Kim, W S, Nassif, N T, Ryce, C, Woods, C G, Michaelis, R C, Tarleton, J, Smith, A
Publicado em 1997

A Multicenter Study on Genotype-Phenotype Correlations in the Fragile X Syndrome, Using Direct Diagnosis with Probe StB12.3: The First 2,253 Cases

Por Rousseau, F., Heitz, D., Tarleton, J., MacPherson, J., Malmgren, H., Dahl, N., Barnicoat, A., Mathew, C., Mornet, E., Tejada, I., Maddalena, A., Spiegel, R., Schinzel, A., Marcos, J. A. G., Schorderet, D. F., Schaap, T., Maccioni, L., Russo, S., Jacobs, P. A., Schwartz, C., Mandel, J. L.
Publicado em 1994