Heterozygosity for Tay-Sachs disease in non-Jewish Americans with ancestry from Ireland or Great Britain.

Author:

van Bael M,Natowicz M R,Tomczak J,Grebner E E,Prence E M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference26 articles.

1. The GM2 gangliosidoses;Gravel, R.A.; Clarke, J.T.R.; Kaback, M.M.; Mahuran, D.; Sandhoff, K.; Suzuki, K.,1995

2. Tay-Sachs disease carrier screening, prenatal diagnosis, and the molecular era. An international perspective, 1970 to;Kaback, M.; Lim-Steele, J.; Dabholkar, D.; Brown, D.; Levy, N.; Zeiger, K.;JAMA,1993

3. A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screening;Triggs-Raine, B.L.; Mules, E.H.; Kaback, M.M.;Am JI Hum Genet,1992

4. Distribution of a pseudodeficiency allele among Tay-Sachs carriers;Tomczak, J.; Boogen, C.; Grebner, E.;Am Hum Genet,1993

5. A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimation;Cao, Z.; Natowicz, M.R.; Kaback, M.M.;Am J Hum Genet,1993

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