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M Kaback

Showing results (31-40 of 114) with videos related to

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Biochemical Genetics|December 1, 1970
Uroporphyrinogen 3 cosynthetase activity in fibroblasts from patients with congenital erythropoietic porphyriaG Romeo, M M Kaback, E Y Levin
Clinical Genetics|April 1, 1977
Chromosome polymorphisms in karyotypes from amniotic fluid cell culturesP E Barker, T Mohandas, M M Kaback
Progress in Clinical and Biological Research|January 1, 1977
Tay-Sachs disease: heterozygote screening and prenatal diagnosis--U.S. experience and world perspectiveM M Kaback, T J Nathan, S Greenwald
Birth Defects Original Article Series|January 1, 1975
Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocationJ Leisti, M M Kaback, D L Rimoin
American Journal of Human Genetics|October 1, 1987
Tay-Sachs disease with hexosaminidase A: characterization of the defective enzyme in two patientsJ Bayleran, P Hechtman, E Kolodny, et al.
Birth Defects Original Article Series|January 1, 1975
The Turner phenotype associated with unbalanced X/autosome translocationJ Leisti, M M Kaback, D L Rimoin
Current Problems in Pediatrics|September 1, 1979
Inherited lipid storage diseases of the central nervous systemA K Percy, L J Shapiro, M M Kaback
Birth Defects Original Article Series|January 1, 1982
Significant of meconium stained fluid in midtrimester amniocentesisL Immken, M Lee, R Stewart, et al.
American Journal of Human Genetics|February 1, 1990
The American Society of Human Genetics statement on cystic fibrosis screeningC T Caskey, M M Kaback, A L Beaudet
Pediatric Research|August 1, 1971
Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cellsM M Kaback, C O Leonard, T H Parmley
Pageof 12

Showing results (31-40 of 114) with videos related to

Sort By:
Pageof 12
Biochemical Genetics|December 1, 1970
Uroporphyrinogen 3 cosynthetase activity in fibroblasts from patients with congenital erythropoietic porphyriaG Romeo, M M Kaback, E Y Levin
Clinical Genetics|April 1, 1977
Chromosome polymorphisms in karyotypes from amniotic fluid cell culturesP E Barker, T Mohandas, M M Kaback
Progress in Clinical and Biological Research|January 1, 1977
Tay-Sachs disease: heterozygote screening and prenatal diagnosis--U.S. experience and world perspectiveM M Kaback, T J Nathan, S Greenwald
Birth Defects Original Article Series|January 1, 1975
Cri-du-chat and trisomy 13 syndromes in an infant with an unbalanced chromosomal translocationJ Leisti, M M Kaback, D L Rimoin
American Journal of Human Genetics|October 1, 1987
Tay-Sachs disease with hexosaminidase A: characterization of the defective enzyme in two patientsJ Bayleran, P Hechtman, E Kolodny, et al.
Birth Defects Original Article Series|January 1, 1975
The Turner phenotype associated with unbalanced X/autosome translocationJ Leisti, M M Kaback, D L Rimoin
Current Problems in Pediatrics|September 1, 1979
Inherited lipid storage diseases of the central nervous systemA K Percy, L J Shapiro, M M Kaback
Birth Defects Original Article Series|January 1, 1982
Significant of meconium stained fluid in midtrimester amniocentesisL Immken, M Lee, R Stewart, et al.
American Journal of Human Genetics|February 1, 1990
The American Society of Human Genetics statement on cystic fibrosis screeningC T Caskey, M M Kaback, A L Beaudet
Pediatric Research|August 1, 1971
Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cellsM M Kaback, C O Leonard, T H Parmley
Pageof 12