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M M Kaback

Showing results (71-80 of 89) with videos related to

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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.
American Journal of Medical Genetics|January 1, 1980
Stimulation of amniotic fluid cell growth by cartilage growth factorM S Golbus, M Djalali, M Klagsbrun, et al.
Science (New York, N.Y.)|October 8, 1971
Xeroderma pigmentosum: a rapid sensitive method for prenatal diagnosisJ D Regan, R B Setlow, M M Kaback, et al.
American Journal of Human Genetics|May 1, 1997
Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs diseaseB R Akerman, M R Natowicz, M M Kaback, et al.
Biochemistry International|July 1, 1992
Ganglioside GM2 levels in human melanoma cells: inverse correlation with lysosomal beta-hexosaminidase A activityD S Hoon, M M Kaback, J Lim-Steele, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Regional mapping of ADA and ITP on human chromosome 20: cytogenetic and somatic cell studies in an X/20 translocationT Mohandas, R S Sparkes, M B Passage, et al.
Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.
American Journal of Obstetrics and Gynecology|December 1, 1974
Second-trimester fetoscopy and fetal blood sampling: current limitations and problemsM D Levine, D E McNeil, M M Kaback, et al.
Pageof 9

Showing results (71-80 of 89) with videos related to

Sort By:
Pageof 9
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.
American Journal of Medical Genetics|January 1, 1980
Stimulation of amniotic fluid cell growth by cartilage growth factorM S Golbus, M Djalali, M Klagsbrun, et al.
Science (New York, N.Y.)|October 8, 1971
Xeroderma pigmentosum: a rapid sensitive method for prenatal diagnosisJ D Regan, R B Setlow, M M Kaback, et al.
American Journal of Human Genetics|May 1, 1997
Novel mutations and DNA-based screening in non-Jewish carriers of Tay-Sachs diseaseB R Akerman, M R Natowicz, M M Kaback, et al.
Biochemistry International|July 1, 1992
Ganglioside GM2 levels in human melanoma cells: inverse correlation with lysosomal beta-hexosaminidase A activityD S Hoon, M M Kaback, J Lim-Steele, et al.
Cytogenetics and Cell Genetics|January 1, 1980
Regional mapping of ADA and ITP on human chromosome 20: cytogenetic and somatic cell studies in an X/20 translocationT Mohandas, R S Sparkes, M B Passage, et al.
Nature Genetics|October 1, 1995
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individualsJ P Struewing, D Abeliovich, T Peretz, et al.
American Journal of Obstetrics and Gynecology|December 1, 1974
Second-trimester fetoscopy and fetal blood sampling: current limitations and problemsM D Levine, D E McNeil, M M Kaback, et al.
Pageof 9