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T Warren

Showing results (171-180 of 471) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reactionBradford Coffee, Kasinathan Muralidharan, William E Highsmith, et al.
Human Genetics|December 1, 1988
Molecular evidence for true isochromosome 21qJ H Priest, R D Blackston, L A Pearse, et al.
Biochemical Society Transactions|May 23, 2018
Mouse models of nesprin-related diseasesCan Zhou, Li Rao, Derek T Warren, et al.
Research in Immunology|July 1, 1995
Bryostatins trigger human polymorphonuclear neutrophil and monocyte oxidative metabolism: association with in vitro antineoplastic activityA H Esa, J T Warren, A D Hess, et al.
Human Molecular Genetics|March 1, 1993
An MspI polymorphism in the hyman serotonin receptor gene (HTR2): detection by DGGE and RFLP analysisJ T Warren, M L Peacock, L C Rodriguez, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Altered synaptic plasticity in a mouse model of fragile X mental retardationKimberly M Huber, Sean M Gallagher, Stephen T Warren, et al.
Pediatric Blood & Cancer|May 5, 2025
Comment on: Use of Plerixafor for Short-Term Management of Leukopenia in a Pediatric Patient With WHIM SyndromeJulia T Warren, Christophe Arbet-Engels, Deborah J Steiner, et al.
Environmental Health Perspectives|October 4, 2002
Developmental toxicology of cadmium in living embryos of a stable transgenic zebrafish lineScott R Blechinger, James T Warren, John Y Kuwada, et al.
Genomics|March 1, 1990
Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reactionS A Ledbetter, D L Nelson, S T Warren, et al.
Human Molecular Genetics|October 1, 1993
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndromeI K Hornstra, D L Nelson, S T Warren, et al.
Pageof 48

Showing results (171-180 of 471) with videos related to

Sort By:
Pageof 48
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular diagnosis of Beckwith-Wiedemann syndrome using quantitative methylation-sensitive polymerase chain reactionBradford Coffee, Kasinathan Muralidharan, William E Highsmith, et al.
Human Genetics|December 1, 1988
Molecular evidence for true isochromosome 21qJ H Priest, R D Blackston, L A Pearse, et al.
Biochemical Society Transactions|May 23, 2018
Mouse models of nesprin-related diseasesCan Zhou, Li Rao, Derek T Warren, et al.
Research in Immunology|July 1, 1995
Bryostatins trigger human polymorphonuclear neutrophil and monocyte oxidative metabolism: association with in vitro antineoplastic activityA H Esa, J T Warren, A D Hess, et al.
Human Molecular Genetics|March 1, 1993
An MspI polymorphism in the hyman serotonin receptor gene (HTR2): detection by DGGE and RFLP analysisJ T Warren, M L Peacock, L C Rodriguez, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Altered synaptic plasticity in a mouse model of fragile X mental retardationKimberly M Huber, Sean M Gallagher, Stephen T Warren, et al.
Pediatric Blood & Cancer|May 5, 2025
Comment on: Use of Plerixafor for Short-Term Management of Leukopenia in a Pediatric Patient With WHIM SyndromeJulia T Warren, Christophe Arbet-Engels, Deborah J Steiner, et al.
Environmental Health Perspectives|October 4, 2002
Developmental toxicology of cadmium in living embryos of a stable transgenic zebrafish lineScott R Blechinger, James T Warren, John Y Kuwada, et al.
Genomics|March 1, 1990
Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequence polymerase chain reactionS A Ledbetter, D L Nelson, S T Warren, et al.
Human Molecular Genetics|October 1, 1993
High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndromeI K Hornstra, D L Nelson, S T Warren, et al.
Pageof 48