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M M Kaback

Showing results (61-70 of 89) with videos related to

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American Journal of Human Genetics|May 1, 1975
Tay-Sachs disease: high gene frequency in a non-Jewish populationT E Kelly, G A Chase, M M Kaback, et al.
American Journal of Human Genetics|October 1, 1990
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening programB H Paw, P T Tieu, M M Kaback, et al.
Journal of the Neurological Sciences|June 1, 1980
Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker)M Zatz, L J Shapiro, D S Campion, et al.
The Journal of Biological Chemistry|September 10, 1984
Faulty association of alpha- and beta-subunits in some forms of beta-hexosaminidase A deficiencyA d'Azzo, R L Proia, E H Kolodny, et al.
The Journal of Pediatrics|June 1, 1973
Gm-gangliosidosis type I: in utero detection and fetal manifestationsM M Kaback, H R Sloan, M Sonneborn, et al.
Prenatal Diagnosis|June 1, 1987
Maternal cell contamination in cultured chorionic villi: comparison of chromosome Q-polymorphisms derived from villi, fetal skin, and maternal lymphocytesJ Williams, A L Medearis, W H Chu, et al.
Journal of Medical Genetics|October 1, 1978
Segregation of an insertional chromosome rearrangement in 3 generationsK E Toomey, T Mohandas, R S Sparkes, et al.
Advances in Experimental Medicine and Biology|January 1, 1972
Further studies on the antenatal detection of sickle cell anemia and other hemoglobinopathiesH H Kazazian, M M Kaback, A P Woodhead, et al.
Birth Defects Original Article Series|January 1, 1977
Prenatal diagnosis of the Meckel syndrome: use of serial ultrasound and alpha-fetoprotein measurementsL J Shapiro, M M Kaback, K E Toomey, et al.
Progress in Clinical and Biological Research|January 1, 1977
Community-based genetic education, communication channels, and knowledge of Tay-Sachs diseaseF Massarik, M M Kaback, S Greenwald, et al.
Pageof 9

Showing results (61-70 of 89) with videos related to

Sort By:
Pageof 9
American Journal of Human Genetics|May 1, 1975
Tay-Sachs disease: high gene frequency in a non-Jewish populationT E Kelly, G A Chase, M M Kaback, et al.
American Journal of Human Genetics|October 1, 1990
Frequency of three Hex A mutant alleles among Jewish and non-Jewish carriers identified in a Tay-Sachs screening programB H Paw, P T Tieu, M M Kaback, et al.
Journal of the Neurological Sciences|June 1, 1980
Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker)M Zatz, L J Shapiro, D S Campion, et al.
The Journal of Biological Chemistry|September 10, 1984
Faulty association of alpha- and beta-subunits in some forms of beta-hexosaminidase A deficiencyA d'Azzo, R L Proia, E H Kolodny, et al.
The Journal of Pediatrics|June 1, 1973
Gm-gangliosidosis type I: in utero detection and fetal manifestationsM M Kaback, H R Sloan, M Sonneborn, et al.
Prenatal Diagnosis|June 1, 1987
Maternal cell contamination in cultured chorionic villi: comparison of chromosome Q-polymorphisms derived from villi, fetal skin, and maternal lymphocytesJ Williams, A L Medearis, W H Chu, et al.
Journal of Medical Genetics|October 1, 1978
Segregation of an insertional chromosome rearrangement in 3 generationsK E Toomey, T Mohandas, R S Sparkes, et al.
Advances in Experimental Medicine and Biology|January 1, 1972
Further studies on the antenatal detection of sickle cell anemia and other hemoglobinopathiesH H Kazazian, M M Kaback, A P Woodhead, et al.
Birth Defects Original Article Series|January 1, 1977
Prenatal diagnosis of the Meckel syndrome: use of serial ultrasound and alpha-fetoprotein measurementsL J Shapiro, M M Kaback, K E Toomey, et al.
Progress in Clinical and Biological Research|January 1, 1977
Community-based genetic education, communication channels, and knowledge of Tay-Sachs diseaseF Massarik, M M Kaback, S Greenwald, et al.
Pageof 9