Diagnostic heteroduplexes: simple detection of carriers of a 4-bp insertion mutation in Tay-Sachs disease.

Por Triggs-Raine, B L, Gravel, R A
Publicado em 1990

Sequence of DNA flanking the exons of the HEXA gene, and identification of mutations in Tay-Sachs disease.

Por Triggs-Raine, B L, Akerman, B R, Clarke, J T, Gravel, R A
Publicado em 1991

Nucleotide sequence of katG, encoding catalase HPI of Escherichia coli.

Por Triggs-Raine, B L, Doble, B W, Mulvey, M R, Sorby, P A, Loewen, P C
Publicado em 1988

A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimation.

Por Cao, Z, Natowicz, M R, Kaback, M M, Lim-Steele, J S, Prence, E M, Brown, D, Chabot, T, Triggs-Raine, B L
Publicado em 1993

A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: Implications for carrier screening

Por Triggs-Raine, B. L., Mules, E. H., Kaback, M. M., Lim-Steele, J. S. T., Dowling, C. E., Akerman, B. R., Natowicz, M. R., Grebner, E. E., Navon, R., Welch, J. P., Greenberg, C. R., Thomas, G. H., Gravel, R. A.
Publicado em 1992