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

door Triggs-Raine, B L, Gravel, R A
Gepubliceerd in 1990

Genotyping an immunodeficiency causing c.1624–11G>A ZAP70 mutation in Canadian Mennonites

door Schroeder, M. L., Triggs-Raine, B., Zelinski, T.
Gepubliceerd in BMC Med Genet (2016)

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

door Triggs-Raine, B L, Akerman, B R, Clarke, J T, Gravel, R A
Gepubliceerd in 1991

Mutational analyses of Tay-Sachs disease: studies on Tay-Sachs carriers of French Canadian background living in New England.

door Triggs-Raine, B, Richard, M, Wasel, N, Prence, E M, Natowicz, M R
Gepubliceerd in 1995

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

door Triggs-Raine, B L, Doble, B W, Mulvey, M R, Sorby, P A, Loewen, P C
Gepubliceerd in 1988

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

door Cao, Z, Natowicz, M R, Kaback, M M, Lim-Steele, J S, Prence, E M, Brown, D, Chabot, T, Triggs-Raine, B L
Gepubliceerd in 1993

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

door 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.
Gepubliceerd in 1992