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M Kaback

Showing results (81-90 of 114) with videos related to

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American Journal of Medical Genetics|September 1, 1991
A 7-year old white-male boy with progressive neurological deteriorationL A Barness, K Henry, P Kling, 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.
American Journal of Medical Genetics|April 1, 1988
Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotypeY Ben-Yoseph, B A Pack, P M Thomas, et al.
American Journal of Medical Genetics|February 1, 1985
Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosisT Mohandas, N Canning, W Chu, et al.
The Journal of Biological Chemistry|June 5, 1990
Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidaseB H Paw, S M Moskowitz, N Uhrhammer, et al.
Pageof 12

Showing results (81-90 of 114) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|September 1, 1991
A 7-year old white-male boy with progressive neurological deteriorationL A Barness, K Henry, P Kling, 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.
American Journal of Medical Genetics|April 1, 1988
Maternal serum hexosaminidase A in pregnancy: effects of gestational age and fetal genotypeY Ben-Yoseph, B A Pack, P M Thomas, et al.
American Journal of Medical Genetics|February 1, 1985
Marker chromosomes: cytogenetic characterization and implications for prenatal diagnosisT Mohandas, N Canning, W Chu, et al.
The Journal of Biological Chemistry|June 5, 1990
Juvenile GM2 gangliosidosis caused by substitution of histidine for arginine at position 499 or 504 of the alpha-subunit of beta-hexosaminidaseB H Paw, S M Moskowitz, N Uhrhammer, et al.
Pageof 12