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S Sparkes

Showing results (151-160 of 355) with videos related to

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Genomics|April 1, 1993
Localization of the gene-encoding upstream stimulatory factor (USF) to human chromosome 1q22-q23B H Shieh, R S Sparkes, R B Gaynor, et al.
Archives of General Psychiatry|June 1, 1988
Association of autism, retinoblastoma, and reduced esterase D activityE R Ritvo, A Mason-Brothers, J H Menkes, et al.
Human Genetics|January 1, 1984
Transferase-deficiency galactosemia: immunochemical studies of the Duarte and Los Angeles variantsM W Andersen, V P Williams, M C Sparkes, et al.
Clinical Orthopaedics and Related Research|November 1, 1984
Hereditary multiple exostoses. Report of a familyB F Crandall, L L Field, R S Sparkes, et al.
Human Genetics|November 1, 1989
Tissue specificity of chromosomal rearrangements in ataxia-telangiectasiaT L Kojis, R R Schreck, R A Gatti, et al.
Archives of Surgery (Chicago, Ill. : 1960)|June 1, 1975
Skin homograft survival in humans after lymphocyte depletion by prolonged thoracic duct drainageS Levine, S Hsu, R S Sparkes, et al.
Genomics|October 1, 1990
Chromosomal distribution of three members of the human natriuretic peptide receptor/guanylyl cyclase gene familyD G Lowe, I Klisak, R S Sparkes, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1980
Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in manT Mohandas, R S Sparkes, B Hellkuhl, et al.
Neurology|April 1, 1986
Genetic linkage studies in Alzheimer's diseaseM A Spence, A Heyman, M L Marazita, et al.
American Journal of Medical Genetics|June 1, 1989
Duplicate report crossing over in Norrie disease familyJ Ngo, M A Spence, V Cortessis, et al.
Pageof 36

Showing results (151-160 of 355) with videos related to

Sort By:
Pageof 36
Genomics|April 1, 1993
Localization of the gene-encoding upstream stimulatory factor (USF) to human chromosome 1q22-q23B H Shieh, R S Sparkes, R B Gaynor, et al.
Archives of General Psychiatry|June 1, 1988
Association of autism, retinoblastoma, and reduced esterase D activityE R Ritvo, A Mason-Brothers, J H Menkes, et al.
Human Genetics|January 1, 1984
Transferase-deficiency galactosemia: immunochemical studies of the Duarte and Los Angeles variantsM W Andersen, V P Williams, M C Sparkes, et al.
Clinical Orthopaedics and Related Research|November 1, 1984
Hereditary multiple exostoses. Report of a familyB F Crandall, L L Field, R S Sparkes, et al.
Human Genetics|November 1, 1989
Tissue specificity of chromosomal rearrangements in ataxia-telangiectasiaT L Kojis, R R Schreck, R A Gatti, et al.
Archives of Surgery (Chicago, Ill. : 1960)|June 1, 1975
Skin homograft survival in humans after lymphocyte depletion by prolonged thoracic duct drainageS Levine, S Hsu, R S Sparkes, et al.
Genomics|October 1, 1990
Chromosomal distribution of three members of the human natriuretic peptide receptor/guanylyl cyclase gene familyD G Lowe, I Klisak, R S Sparkes, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1980
Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in manT Mohandas, R S Sparkes, B Hellkuhl, et al.
Neurology|April 1, 1986
Genetic linkage studies in Alzheimer's diseaseM A Spence, A Heyman, M L Marazita, et al.
American Journal of Medical Genetics|June 1, 1989
Duplicate report crossing over in Norrie disease familyJ Ngo, M A Spence, V Cortessis, et al.
Pageof 36