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American Journal of Human Genetics
|
February 1, 1992
General population screening for cystic fibrosis is premature
L Biesecker, B Bowles-Biesecker, F Collins, et al.
Progress in Medical Genetics
|
January 1, 1974
Approaches to the control and prevention of Tay-Sachs disease
M M Kaback, R S Zeiger, L W Reynolds, et al.
Social Science & Medicine
|
May 1, 1977
Health behavior and genetic screening for carriers of Tay-Sachs disease: a prospective study
M S Goldstein, S Greenwald, T Nathan, et al.
Journal of Community Health
|
January 1, 1975
Some influences on public participation in a genetic screening program
M H Becker, M M Kaback, I M Rosenstock, et al.
Human Mutation
|
January 1, 1994
The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population
M A Whitney, P Jakobs, M Kaback, et al.
Archives of Neurology
|
June 1, 1973
Ultrastructure manifestations of G M1 and G M2 gangliosidosis in fetal tissues
A K Percy, U M McCormick, M M Kaback, et al.
Clinical Genetics
|
November 1, 1977
Further delineation of the supernumerary chromosome in the Cat-Eye syndrome
K E Toomey, T Mohandas, J Leisti, et al.
Birth Defects Original Article Series
|
January 1, 1976
Allelic mutations in the mucopolysaccharidoses
J Leisti, D L Rimoin, M Kaback, et al.
American Journal of Human Genetics
|
November 1, 1973
Globoid cell (Krabbe's) leukodystrophy: heterozygote detection in cultured skin fibroblasts
D F Farrell, A K Percy, M M Kaback, et al.
Journal of the Neurological Sciences
|
May 1, 1978
Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in progressive muscular dystrophies
M Zatz, L J Shapiro, D S Campion, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 114) with videos related to
Sort By:
Page
of 12
American Journal of Human Genetics
|
February 1, 1992
General population screening for cystic fibrosis is premature
L Biesecker, B Bowles-Biesecker, F Collins, et al.
Progress in Medical Genetics
|
January 1, 1974
Approaches to the control and prevention of Tay-Sachs disease
M M Kaback, R S Zeiger, L W Reynolds, et al.
Social Science & Medicine
|
May 1, 1977
Health behavior and genetic screening for carriers of Tay-Sachs disease: a prospective study
M S Goldstein, S Greenwald, T Nathan, et al.
Journal of Community Health
|
January 1, 1975
Some influences on public participation in a genetic screening program
M H Becker, M M Kaback, I M Rosenstock, et al.
Human Mutation
|
January 1, 1994
The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population
M A Whitney, P Jakobs, M Kaback, et al.
Archives of Neurology
|
June 1, 1973
Ultrastructure manifestations of G M1 and G M2 gangliosidosis in fetal tissues
A K Percy, U M McCormick, M M Kaback, et al.
Clinical Genetics
|
November 1, 1977
Further delineation of the supernumerary chromosome in the Cat-Eye syndrome
K E Toomey, T Mohandas, J Leisti, et al.
Birth Defects Original Article Series
|
January 1, 1976
Allelic mutations in the mucopolysaccharidoses
J Leisti, D L Rimoin, M Kaback, et al.
American Journal of Human Genetics
|
November 1, 1973
Globoid cell (Krabbe's) leukodystrophy: heterozygote detection in cultured skin fibroblasts
D F Farrell, A K Percy, M M Kaback, et al.
Journal of the Neurological Sciences
|
May 1, 1978
Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in progressive muscular dystrophies
M Zatz, L J Shapiro, D S Campion, et al.
Page
of 12