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M M Kaback

Showing results (51-60 of 89) with videos related to

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Social Science & Medicine|May 1, 1977
Health behavior and genetic screening for carriers of Tay-Sachs disease: a prospective studyM S Goldstein, S Greenwald, T Nathan, et al.
Journal of Community Health|January 1, 1975
Some influences on public participation in a genetic screening programM 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 tissuesA 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 syndromeK 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 fibroblastsD 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 dystrophiesM 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 testD 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 cellsW A Carter, K R Hande, B Essien, et al.
Birth Defects Original Article Series|January 1, 1975
Diagnosis of skeletal dysplasias in second trimester fetusesM 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 abortionB D Blumberg, J D Shulkin, J I Rotter, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
Social Science & Medicine|May 1, 1977
Health behavior and genetic screening for carriers of Tay-Sachs disease: a prospective studyM S Goldstein, S Greenwald, T Nathan, et al.
Journal of Community Health|January 1, 1975
Some influences on public participation in a genetic screening programM 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 tissuesA 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 syndromeK 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 fibroblastsD 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 dystrophiesM 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 testD 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 cellsW A Carter, K R Hande, B Essien, et al.
Birth Defects Original Article Series|January 1, 1975
Diagnosis of skeletal dysplasias in second trimester fetusesM 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 abortionB D Blumberg, J D Shulkin, J I Rotter, et al.
Pageof 9