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Biochimica Et Biophysica Acta
|
July 10, 1997
Palmitoyl-protein thioesterase deficiency in fibroblasts of individuals with infantile neuronal ceroid lipofuscinosis and I-cell disease
L A Verkruyse, M R Natowicz, S L Hofmann
American Journal of Medical Genetics
|
January 2, 1996
EEOC compliance manual for the ADA and genetic discrimination
J S Alper, J K Alper, M R Natowicz
American Journal of Human Genetics
|
October 1, 1992
Genetic discrimination and the Americans with Disabilities Act
M R Natowicz, J K Alper, J S Alper
Journal of Child Neurology
|
March 1, 1995
Delayed myelination in infants and young children: radiographic and clinical correlates
L A Squires, K S Krishnamoorthy, M R Natowicz
The Journal of Biological Chemistry
|
February 16, 1996
Glucuronic acid-conjugated dihydroxy fatty acids in the urine of patients with generalized peroxisomal disorders
J M Street, J E Evans, M R Natowicz
American Journal of Human Genetics
|
August 1, 1993
Genetic conditions and the scope of the Americans with Disabilities Act
M R Natowicz, J K Alper, J S Alper
American Journal of Human Genetics
|
July 1, 1992
Molecular diagnostics for myelin proteolipid protein gene mutations in Pelizaeus-Merzbacher disease
R Doll, M R Natowicz, R Schiffmann, et al.
American Journal of Medical Genetics
|
May 8, 1995
Tay-Sachs disease in persons of French-Canadian heritage in northern New England
G E Palomaki, J Williams, J E Haddow, et al.
Methods in Enzymology
|
November 24, 1999
Analysis of sulfatide and enzymes of sulfatide metabolism
F B Jungalwala, M R Natowicz, P Chaturvedi, et al.
Clinical Pediatrics
|
April 1, 1995
Marked heterogeneity in Niemann-Pick disease, type C. Clinical and ultrastructural findings
M R Natowicz, J M Stoler, E M Prence, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Biochimica Et Biophysica Acta
|
July 10, 1997
Palmitoyl-protein thioesterase deficiency in fibroblasts of individuals with infantile neuronal ceroid lipofuscinosis and I-cell disease
L A Verkruyse, M R Natowicz, S L Hofmann
American Journal of Medical Genetics
|
January 2, 1996
EEOC compliance manual for the ADA and genetic discrimination
J S Alper, J K Alper, M R Natowicz
American Journal of Human Genetics
|
October 1, 1992
Genetic discrimination and the Americans with Disabilities Act
M R Natowicz, J K Alper, J S Alper
Journal of Child Neurology
|
March 1, 1995
Delayed myelination in infants and young children: radiographic and clinical correlates
L A Squires, K S Krishnamoorthy, M R Natowicz
The Journal of Biological Chemistry
|
February 16, 1996
Glucuronic acid-conjugated dihydroxy fatty acids in the urine of patients with generalized peroxisomal disorders
J M Street, J E Evans, M R Natowicz
American Journal of Human Genetics
|
August 1, 1993
Genetic conditions and the scope of the Americans with Disabilities Act
M R Natowicz, J K Alper, J S Alper
American Journal of Human Genetics
|
July 1, 1992
Molecular diagnostics for myelin proteolipid protein gene mutations in Pelizaeus-Merzbacher disease
R Doll, M R Natowicz, R Schiffmann, et al.
American Journal of Medical Genetics
|
May 8, 1995
Tay-Sachs disease in persons of French-Canadian heritage in northern New England
G E Palomaki, J Williams, J E Haddow, et al.
Methods in Enzymology
|
November 24, 1999
Analysis of sulfatide and enzymes of sulfatide metabolism
F B Jungalwala, M R Natowicz, P Chaturvedi, et al.
Clinical Pediatrics
|
April 1, 1995
Marked heterogeneity in Niemann-Pick disease, type C. Clinical and ultrastructural findings
M R Natowicz, J M Stoler, E M Prence, et al.
Page
of 6