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Biochemical Genetics
|
December 1, 1970
Uroporphyrinogen 3 cosynthetase activity in fibroblasts from patients with congenital erythropoietic porphyria
G Romeo, M M Kaback, E Y Levin
Clinical Genetics
|
April 1, 1977
Chromosome polymorphisms in karyotypes from amniotic fluid cell cultures
P 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 perspective
M 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 translocation
J 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 patients
J Bayleran, P Hechtman, E Kolodny, et al.
Birth Defects Original Article Series
|
January 1, 1975
The Turner phenotype associated with unbalanced X/autosome translocation
J Leisti, M M Kaback, D L Rimoin
Current Problems in Pediatrics
|
September 1, 1979
Inherited lipid storage diseases of the central nervous system
A K Percy, L J Shapiro, M M Kaback
Birth Defects Original Article Series
|
January 1, 1982
Significant of meconium stained fluid in midtrimester amniocentesis
L 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 screening
C 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 cells
M M Kaback, C O Leonard, T H Parmley
Page
of 12
Search research articles
Search
Showing results (31-40 of 114) with videos related to
Sort By:
Page
of 12
Biochemical Genetics
|
December 1, 1970
Uroporphyrinogen 3 cosynthetase activity in fibroblasts from patients with congenital erythropoietic porphyria
G Romeo, M M Kaback, E Y Levin
Clinical Genetics
|
April 1, 1977
Chromosome polymorphisms in karyotypes from amniotic fluid cell cultures
P 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 perspective
M 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 translocation
J 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 patients
J Bayleran, P Hechtman, E Kolodny, et al.
Birth Defects Original Article Series
|
January 1, 1975
The Turner phenotype associated with unbalanced X/autosome translocation
J Leisti, M M Kaback, D L Rimoin
Current Problems in Pediatrics
|
September 1, 1979
Inherited lipid storage diseases of the central nervous system
A K Percy, L J Shapiro, M M Kaback
Birth Defects Original Article Series
|
January 1, 1982
Significant of meconium stained fluid in midtrimester amniocentesis
L 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 screening
C 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 cells
M M Kaback, C O Leonard, T H Parmley
Page
of 12