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Acta Paediatrica Japonica : Overseas Edition
|
June 1, 1996
Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1
H Ida, O M Rennert, T Ito, et al.
Human Genetics
|
September 10, 1999
Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation
H Ida, O M Rennert, K Iwasawa, et al.
Physiological Chemistry and Physics and Medical NMR
|
January 1, 1983
Polyamine metabolism in McCoy cells: I. Comparative studies of extracellular polyamine conjugated proteins of human fibroblast and McCoy cultures
M Z Fan, W Y Chan, G Griesmann, et al.
American Journal of Medical Genetics
|
July 1, 1988
Atypical Menkes steely hair disease
J A Westman, D C Richardson, O M Rennert, et al.
Science (New York, N.Y.)
|
April 18, 1980
Genetic expression of Wilson's disease in cell culture: a diagnostic marker
W Y Chan, W Cushing, M A Coffman, et al.
Journal of Neurochemistry
|
February 1, 1979
Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency
Y Eto, M Owada, T Kitagawa, et al.
Pharmacology, Biochemistry, and Behavior
|
April 1, 1984
Interstrain variation in acute toxic response to caffeine among inbred mice
T W Seale, P Johnson, J M Carney, et al.
Maryland Medical Journal (Baltimore, Md. : 1985)
|
March 1, 1995
Molecular genetics in pediatric training: how much do we really know?
C A Stratakis, N J Cavuto, D Nelson, et al.
Pediatric Research
|
March 1, 1977
Ornithine decarboxylase and S-adenosyl methionine decarboxylase in skin fibroblasts of normal and cystic fibrosis patients
B Buehler, R Wright, S Schott, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 2, 1981
Urinary polyamines in preterm infants
M Perlman, W Y Chan, T Z Ramadan, et al.
Page
of 25
Search research articles
Search
Showing results (131-140 of 250) with videos related to
Sort By:
Page
of 25
Acta Paediatrica Japonica : Overseas Edition
|
June 1, 1996
Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1
H Ida, O M Rennert, T Ito, et al.
Human Genetics
|
September 10, 1999
Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutation
H Ida, O M Rennert, K Iwasawa, et al.
Physiological Chemistry and Physics and Medical NMR
|
January 1, 1983
Polyamine metabolism in McCoy cells: I. Comparative studies of extracellular polyamine conjugated proteins of human fibroblast and McCoy cultures
M Z Fan, W Y Chan, G Griesmann, et al.
American Journal of Medical Genetics
|
July 1, 1988
Atypical Menkes steely hair disease
J A Westman, D C Richardson, O M Rennert, et al.
Science (New York, N.Y.)
|
April 18, 1980
Genetic expression of Wilson's disease in cell culture: a diagnostic marker
W Y Chan, W Cushing, M A Coffman, et al.
Journal of Neurochemistry
|
February 1, 1979
Neurochemical abnormality in I-cell disease: chemical analysis and a possible importance of beta-galactosidase deficiency
Y Eto, M Owada, T Kitagawa, et al.
Pharmacology, Biochemistry, and Behavior
|
April 1, 1984
Interstrain variation in acute toxic response to caffeine among inbred mice
T W Seale, P Johnson, J M Carney, et al.
Maryland Medical Journal (Baltimore, Md. : 1985)
|
March 1, 1995
Molecular genetics in pediatric training: how much do we really know?
C A Stratakis, N J Cavuto, D Nelson, et al.
Pediatric Research
|
March 1, 1977
Ornithine decarboxylase and S-adenosyl methionine decarboxylase in skin fibroblasts of normal and cystic fibrosis patients
B Buehler, R Wright, S Schott, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 2, 1981
Urinary polyamines in preterm infants
M Perlman, W Y Chan, T Z Ramadan, et al.
Page
of 25