Zobrazeno 1 - 10
of 120
pro vyhledávání: '"KABACK, M. M."'
We have evaluated the feasibility of using PCR-based mutation screening for non-Jewish enzyme-defined carriers identified through Tay-Sachs disease-prevention programs. Although Tay-Sachs mutations are rare in the general population, non-Jewish indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::64665c6c27fed31af9a7cc8533f82134
https://europepmc.org/articles/PMC1712448/
https://europepmc.org/articles/PMC1712448/
Publikováno v:
Journal of Medical Genetics; Oct1978, Vol. 15 Issue 5, p382-387, 6p, 5 Black and White Photographs, 2 Diagrams, 1 Chart
Publikováno v:
Neurology; Oct1977, Vol. 27 Issue 10, p933-941, 9p
Autor:
Williams, John, Medearis, Arnold L., Chu, Weimei H., Kovacs, George D., Kaback, Michael M., Williams, J 3rd, Medearis, A L, Chu, W H, Kovacs, G D, Kaback, M M
Publikováno v:
Prenatal Diagnosis; Jun1987, Vol. 7 Issue 5, p315-322, 8p
Publikováno v:
Prenatal Diagnosis; Jan1982, Vol. 2 Issue 1, p25-31, 7p
Autor:
Akerman, B. R., Zielenski, J., Triggs-Raine, B. L., Prence, E. M., Natowicz, M. R., Lim-Steele, J. S. T., Kaback, M. M., Mules, E. H., Thomas, G. H., Clarke, J. T. R., Gravel, R. A.
Publikováno v:
Human Mutation; 1992, Vol. 1 Issue 4, p303-309, 7p
Autor:
Kaback, Michael M., Kaback, M M
Publikováno v:
International Journal of Technology Assessment in Health Care; Oct1994, Vol. 10 Issue 4, p592-603, 12p
Publikováno v:
Clinical Genetics; Nov1977, Vol. 12 Issue 5, p275-284, 10p
Publikováno v:
Clinical Genetics; Mar1977, Vol. 11 Issue 3, p243-248, 6p