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R S SPARKES

Showing results (51-60 of 272) with videos related to

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Investigative Ophthalmology & Visual Science|May 1, 1984
Aniridia: enzyme studies in an 11p--chromosomal deletionJ B Bateman, M C Sparkes, R S Sparkes
Science (New York, N.Y.)|September 8, 1978
Bone marrow origin of hepatic macrophages (Kupffer cells) in humansR P Gale, R S Sparkes, D W Golde
American Journal of Medical Genetics|January 1, 1980
C-band polymorphism: comparison between trisomy 21 cases and mentally retarded controlsS J Funderburk, I Klisak, R S Sparkes, et al.
Journal of Medical Genetics|December 1, 1980
Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotypeB M Lippe, R S Sparkes, B Fass, et al.
Kroc Foundation Series|January 1, 1985
Genetic linkage studies in ataxia-telangiectasia: Gm markersR A Gatti, M Boehnke, M Crist, et al.
American Journal of Hematology|May 1, 1993
Ph1-chromosome positive acute lymphoblastic leukemia: is t(9;22) the initial abnormality?I Aurer, R S Sparkes, G Schiller, et al.
American Journal of Human Genetics|September 1, 1984
The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressedL Immken, T Mohandas, R S Sparkes, et al.
Blood|December 1, 1981
Somatic cell hybrid analyses of hematopoietic differentiationH P Koeffler, R S Sparkes, R Billing, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1981
Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16H P Koeffler, R S Sparkes, H Stang, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 1, 1986
Congenital ocular fibrosis syndrome associated with the Prader-Willi syndromeB Kalpakian, J B Bateman, R S Sparkes, et al.
Pageof 28

Showing results (51-60 of 272) with videos related to

Sort By:
Pageof 28
Investigative Ophthalmology & Visual Science|May 1, 1984
Aniridia: enzyme studies in an 11p--chromosomal deletionJ B Bateman, M C Sparkes, R S Sparkes
Science (New York, N.Y.)|September 8, 1978
Bone marrow origin of hepatic macrophages (Kupffer cells) in humansR P Gale, R S Sparkes, D W Golde
American Journal of Medical Genetics|January 1, 1980
C-band polymorphism: comparison between trisomy 21 cases and mentally retarded controlsS J Funderburk, I Klisak, R S Sparkes, et al.
Journal of Medical Genetics|December 1, 1980
Craniosynostosis and syndactyly: expanding the 11q-- chromosomal deletion phenotypeB M Lippe, R S Sparkes, B Fass, et al.
Kroc Foundation Series|January 1, 1985
Genetic linkage studies in ataxia-telangiectasia: Gm markersR A Gatti, M Boehnke, M Crist, et al.
American Journal of Hematology|May 1, 1993
Ph1-chromosome positive acute lymphoblastic leukemia: is t(9;22) the initial abnormality?I Aurer, R S Sparkes, G Schiller, et al.
American Journal of Human Genetics|September 1, 1984
The steroid sulfatase locus on structurally abnormal inactive X chromosomes is expressedL Immken, T Mohandas, R S Sparkes, et al.
Blood|December 1, 1981
Somatic cell hybrid analyses of hematopoietic differentiationH P Koeffler, R S Sparkes, R Billing, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1981
Regional assignment of genes for human alpha-globin and phosphoglycollate phosphatase to the short arm of chromosome 16H P Koeffler, R S Sparkes, H Stang, et al.
Journal of Pediatric Ophthalmology and Strabismus|July 1, 1986
Congenital ocular fibrosis syndrome associated with the Prader-Willi syndromeB Kalpakian, J B Bateman, R S Sparkes, et al.
Pageof 28