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Journal of Molecular Biology
|
August 25, 1974
Globin gene expression in cultured erythroleukemic cells
J Ross, J Gielen, S Packman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Abnormal fatty acid composition of biotin-responsive multiple carboxylase deficiency fibroblasts
S Packman, S C Whitney, M Fitch, et al.
Biochemistry
|
June 29, 1976
Purification and translation of an immunoglobulin lambda chain messenger RNA from mouse myeloma
T Honjo, D Swan, S Packman, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
Psychological complications of patients with Gaucher disease
W Packman, T Wilson Crosbie, A Riesner, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2003
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes
X Fu, P Rinaldo, S H Hahn, et al.
Journal of the American Academy of Dermatology
|
February 1, 1993
Dermatitis in treated maple syrup urine disease
S E Koch, S Packman, T K Koch, et al.
Advances in Experimental Medicine and Biology
|
June 1, 1974
DNA complementary to globin and immunoglobulin mRNA: a probe to study gene expression
H Aviv, S Packman, J Ross, et al.
Human Molecular Genetics
|
November 1, 1996
A repeated element in the regulatory region of the MNK gene and its deletion in a patient with occipital horn syndrome
B Levinson, R Conant, R Schnur, et al.
American Journal of Human Genetics
|
November 1, 1994
Diverse mutations in patients with Menkes disease often lead to exon skipping
S Das, B Levinson, S Whitney, et al.
The Journal of Pediatrics
|
September 1, 1996
Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapy
M H Fries, P Rinaldo, E Schmidt-Sommerfeld, et al.
Page
of 10
Search research articles
Search
Showing results (41-50 of 98) with videos related to
Sort By:
Page
of 10
Journal of Molecular Biology
|
August 25, 1974
Globin gene expression in cultured erythroleukemic cells
J Ross, J Gielen, S Packman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1989
Abnormal fatty acid composition of biotin-responsive multiple carboxylase deficiency fibroblasts
S Packman, S C Whitney, M Fitch, et al.
Biochemistry
|
June 29, 1976
Purification and translation of an immunoglobulin lambda chain messenger RNA from mouse myeloma
T Honjo, D Swan, S Packman, et al.
Journal of Inherited Metabolic Disease
|
April 8, 2006
Psychological complications of patients with Gaucher disease
W Packman, T Wilson Crosbie, A Riesner, et al.
Journal of Inherited Metabolic Disease
|
July 23, 2003
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes
X Fu, P Rinaldo, S H Hahn, et al.
Journal of the American Academy of Dermatology
|
February 1, 1993
Dermatitis in treated maple syrup urine disease
S E Koch, S Packman, T K Koch, et al.
Advances in Experimental Medicine and Biology
|
June 1, 1974
DNA complementary to globin and immunoglobulin mRNA: a probe to study gene expression
H Aviv, S Packman, J Ross, et al.
Human Molecular Genetics
|
November 1, 1996
A repeated element in the regulatory region of the MNK gene and its deletion in a patient with occipital horn syndrome
B Levinson, R Conant, R Schnur, et al.
American Journal of Human Genetics
|
November 1, 1994
Diverse mutations in patients with Menkes disease often lead to exon skipping
S Das, B Levinson, S Whitney, et al.
The Journal of Pediatrics
|
September 1, 1996
Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapy
M H Fries, P Rinaldo, E Schmidt-Sommerfeld, et al.
Page
of 10