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Social Science & Medicine
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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.
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.
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.
Human Mutation
|
January 1, 1995
A novel mutation at the invariant acceptor splice site of intron 9 in the HEXA gene [IVS9-1 G-->T] detected by a PCR-based diagnostic test
D H Brown, B L Triggs-Raine, M J McGinniss, et al.
Infection and Immunity
|
May 1, 1971
Comparative production of interferon by human fetal, neonatal, and maternal cells
W A Carter, K R Hande, B Essien, et al.
Birth Defects Original Article Series
|
January 1, 1975
Diagnosis of skeletal dysplasias in second trimester fetuses
M D Levine, R Lachman, D L Rimoin, et al.
American Journal of Human Genetics
|
November 1, 1982
Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion
B D Blumberg, J D Shulkin, J I Rotter, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 89) with videos related to
Sort By:
Page
of 9
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.
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.
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.
Human Mutation
|
January 1, 1995
A novel mutation at the invariant acceptor splice site of intron 9 in the HEXA gene [IVS9-1 G-->T] detected by a PCR-based diagnostic test
D H Brown, B L Triggs-Raine, M J McGinniss, et al.
Infection and Immunity
|
May 1, 1971
Comparative production of interferon by human fetal, neonatal, and maternal cells
W A Carter, K R Hande, B Essien, et al.
Birth Defects Original Article Series
|
January 1, 1975
Diagnosis of skeletal dysplasias in second trimester fetuses
M D Levine, R Lachman, D L Rimoin, et al.
American Journal of Human Genetics
|
November 1, 1982
Minor chromosomal variants and major chromosomal anomalies in couples with recurrent abortion
B D Blumberg, J D Shulkin, J I Rotter, et al.
Page
of 9