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G N Donnell

Showing results (21-30 of 73) with videos related to

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Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|September 1, 1976
Differential fluorescence of sister chromatids with 4'-6-diamidino-2-phenylindoleM S Lin, O S Alfi, G N Donnell
Journal of Medical Genetics|June 1, 1973
Partial trisomy of the long arm of chromosome No. 7O S Alfi, G N Donnell, S L Kramer
Pediatric Radiology|January 1, 1977
Radiographic features of fucosidosisF A Lee, G N Donnell, J L Gwinn
Ophthalmology|June 1, 1979
Ocular findings in cytogenetic syndromesW A Wilson, O S Alfi, G N Donnell
The Journal of Urology|October 1, 1970
Reifenstein's syndrome: hereditary familial hypogonadism with hypospadias and gynecomastiaL W Jones, H Isaacs, H Edelbrock, et al.
Pediatrics|September 1, 1972
Intellectual and personality development in children with galactosemiaK Fishler, G N Donnell, W R Bergren, et al.
Annales De Genetique|March 1, 1976
The 9p- syndromeO S Alfi, G N Donnell, P W Allderdice, et al.
Perspectives in Pediatric Pathology|January 1, 1979
Fibroblast culture in the diagnosis of genetic metabolic diseases: comparative histochemical, ultrastructural, and biochemical studiesB H Landing, W G Ng, O Alfi, et al.
The Journal of Pediatrics|July 1, 1989
Milk produced by mothers with galactosemiaW G Ng, Y K Xu, F Kaufman, et al.
The American Journal of Medicine|February 1, 1970
Disorder of purine metabolism due to partial deficiency of hypoxanthine-guanine phosphoribosyltransferase. A study of a familyM D Kogut, G N Donnell, W L Nyhan, et al.
Pageof 8

Showing results (21-30 of 73) with videos related to

Sort By:
Pageof 8
Canadian Journal of Genetics and Cytology. Journal Canadien De Genetique Et De Cytologie|September 1, 1976
Differential fluorescence of sister chromatids with 4'-6-diamidino-2-phenylindoleM S Lin, O S Alfi, G N Donnell
Journal of Medical Genetics|June 1, 1973
Partial trisomy of the long arm of chromosome No. 7O S Alfi, G N Donnell, S L Kramer
Pediatric Radiology|January 1, 1977
Radiographic features of fucosidosisF A Lee, G N Donnell, J L Gwinn
Ophthalmology|June 1, 1979
Ocular findings in cytogenetic syndromesW A Wilson, O S Alfi, G N Donnell
The Journal of Urology|October 1, 1970
Reifenstein's syndrome: hereditary familial hypogonadism with hypospadias and gynecomastiaL W Jones, H Isaacs, H Edelbrock, et al.
Pediatrics|September 1, 1972
Intellectual and personality development in children with galactosemiaK Fishler, G N Donnell, W R Bergren, et al.
Annales De Genetique|March 1, 1976
The 9p- syndromeO S Alfi, G N Donnell, P W Allderdice, et al.
Perspectives in Pediatric Pathology|January 1, 1979
Fibroblast culture in the diagnosis of genetic metabolic diseases: comparative histochemical, ultrastructural, and biochemical studiesB H Landing, W G Ng, O Alfi, et al.
The Journal of Pediatrics|July 1, 1989
Milk produced by mothers with galactosemiaW G Ng, Y K Xu, F Kaufman, et al.
The American Journal of Medicine|February 1, 1970
Disorder of purine metabolism due to partial deficiency of hypoxanthine-guanine phosphoribosyltransferase. A study of a familyM D Kogut, G N Donnell, W L Nyhan, et al.
Pageof 8