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G N Donnell

Showing results (31-40 of 73) with videos related to

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American Journal of Human Genetics|January 1, 1976
Biochemical and genetic studies of plasma and leukocyte alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
Birth Defects Original Article Series|January 1, 1975
Urinary alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
American Journal of Diseases of Children (1960)|January 1, 1985
Beta-glucuronidase deficiency. A heterogeneous mucopolysaccharidosisJ E Lee, R E Falk, W G Ng, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Deficit of uridine diphosphate galactose in galactosaemiaW G Ng, Y K Xu, F R Kaufman, et al.
Science (New York, N.Y.)|May 12, 1972
Galactonic Acid in galactosemia: identification in the urineW R Bergren, W G Ng, G N Donnell, et al.
Biochemical Medicine|April 1, 1973
Urinary galactitol in galactosemic patientsT F Roe, W G Ng, W R Bergren, et al.
Annales De Genetique|March 1, 1973
Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndromeO Alfi, G N Donnell, B F Crandall, et al.
Birth Defects Original Article Series|January 1, 1974
46, Del (9) (22:), a new deletion syndromeO S Alfi, R G Sanger, A E Sweeny, et al.
Clinical Pediatrics|January 1, 1973
A short, retarded child with a deletion of the short arm of chromosome 18 (18p-)C E Parker, G N Donnell, J Mavalwala, et al.
The Journal of Pediatrics|June 1, 1971
Childbearing by a galactosemic womanT F Roe, J G Hallatt, G N Donnell, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|January 1, 1976
Biochemical and genetic studies of plasma and leukocyte alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
Birth Defects Original Article Series|January 1, 1975
Urinary alpha-L-fucosidaseW G Ng, G N Donnell, R Koch, et al.
American Journal of Diseases of Children (1960)|January 1, 1985
Beta-glucuronidase deficiency. A heterogeneous mucopolysaccharidosisJ E Lee, R E Falk, W G Ng, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Deficit of uridine diphosphate galactose in galactosaemiaW G Ng, Y K Xu, F R Kaufman, et al.
Science (New York, N.Y.)|May 12, 1972
Galactonic Acid in galactosemia: identification in the urineW R Bergren, W G Ng, G N Donnell, et al.
Biochemical Medicine|April 1, 1973
Urinary galactitol in galactosemic patientsT F Roe, W G Ng, W R Bergren, et al.
Annales De Genetique|March 1, 1973
Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndromeO Alfi, G N Donnell, B F Crandall, et al.
Birth Defects Original Article Series|January 1, 1974
46, Del (9) (22:), a new deletion syndromeO S Alfi, R G Sanger, A E Sweeny, et al.
Clinical Pediatrics|January 1, 1973
A short, retarded child with a deletion of the short arm of chromosome 18 (18p-)C E Parker, G N Donnell, J Mavalwala, et al.
The Journal of Pediatrics|June 1, 1971
Childbearing by a galactosemic womanT F Roe, J G Hallatt, G N Donnell, et al.
Pageof 8