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M M Kaback

Showing results (81-90 of 89) with videos related to

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Lancet (London, England)|June 14, 1975
Letter: Phenotypic variation in alpha-L-iduronidase deficiencyJ Leisti, D L Rimoin, M M Kaback, et al.
American Journal of Human Genetics|November 1, 1981
Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophyR L Stevens, A L Fluharty, H Kihara, et al.
American Journal of Human Genetics|December 1, 1993
A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimationZ Cao, M R Natowicz, M M Kaback, et al.
Pediatric Research|October 1, 1979
Metachromatic leukodystrophy without arylsulfatase A deficiencyL J Shapiro, K A Aleck, M M Kaback, et al.
Journal of Medical Genetics|June 1, 1993
Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British IslesE C Landels, P M Green, I H Ellis, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
Human Mutation|January 1, 1992
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studiesB R Akerman, J Zielenski, B L Triggs-Raine, et al.
American Journal of Human Genetics|October 1, 1992
A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.
American Journal of Medical Genetics|December 31, 1997
Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical GeneticsC J Curry, R E Stevenson, D Aughton, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Lancet (London, England)|June 14, 1975
Letter: Phenotypic variation in alpha-L-iduronidase deficiencyJ Leisti, D L Rimoin, M M Kaback, et al.
American Journal of Human Genetics|November 1, 1981
Cerebroside sulfatase activator deficiency induced metachromatic leukodystrophyR L Stevens, A L Fluharty, H Kihara, et al.
American Journal of Human Genetics|December 1, 1993
A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimationZ Cao, M R Natowicz, M M Kaback, et al.
Pediatric Research|October 1, 1979
Metachromatic leukodystrophy without arylsulfatase A deficiencyL J Shapiro, K A Aleck, M M Kaback, et al.
Journal of Medical Genetics|June 1, 1993
Further investigation of the HEXA gene intron 9 donor splice site mutation frequently found in non-Jewish Tay-Sachs disease patients from the British IslesE C Landels, P M Green, I H Ellis, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
Human Mutation|January 1, 1992
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studiesB R Akerman, J Zielenski, B L Triggs-Raine, et al.
American Journal of Human Genetics|October 1, 1992
A pseudodeficiency allele common in non-Jewish Tay-Sachs carriers: implications for carrier screeningB L Triggs-Raine, E H Mules, M M Kaback, et al.
American Journal of Medical Genetics|December 31, 1997
Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical GeneticsC J Curry, R E Stevenson, D Aughton, et al.
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