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Showing results (971-980 of 1,307) with videos related to

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Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.
Annals of Neurology|March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysisL J Ptacek, L Gouw, H Kwieciński, et al.
Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.
The Journal of Experimental Medicine|November 13, 2008
Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysisRobbert M Spaapen, Henk M Lokhorst, Kelly van den Oudenalder, et al.
Journal of Endourology|September 2, 2020
Evaluation of Patient Treatment Preferences for 15 to 20 mm Kidney Stones: A Conjoint AnalysisKyle Spradling, Hriday P Bhambhvani, Timothy Chang, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 13, 2019
Twenty-Four Hour Urine Testing and Prescriptions for Urinary Stone Disease-Related Medications in VeteransShen Song, I-Chun Thomas, Calyani Ganesan, et al.
Nucleic Acids Research|March 24, 2017
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicingSole Gatto, Miriam Gagliardi, Monica Franzese, et al.
American Journal of Human Genetics|October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2M Horwitz, K F Benson, F Q Li, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Journal of Medical Genetics|June 5, 2010
Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancerDeborah W Neklason, Thérèse M Tuohy, Jeffery Stevens, et al.
Pageof 131

Showing results (971-980 of 1,307) with videos related to

Sort By:
Pageof 131
Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.
Annals of Neurology|March 1, 1993
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysisL J Ptacek, L Gouw, H Kwieciński, et al.
Genomics|November 1, 1992
Linkage studies of Usher syndrome type 1: exclusion results from the Usher syndrome consortiumB J Keats, A A Todorov, L D Atwood, et al.
The Journal of Experimental Medicine|November 13, 2008
Toward targeting B cell cancers with CD4+ CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysisRobbert M Spaapen, Henk M Lokhorst, Kelly van den Oudenalder, et al.
Journal of Endourology|September 2, 2020
Evaluation of Patient Treatment Preferences for 15 to 20 mm Kidney Stones: A Conjoint AnalysisKyle Spradling, Hriday P Bhambhvani, Timothy Chang, et al.
Clinical Journal of the American Society of Nephrology : CJASN|November 13, 2019
Twenty-Four Hour Urine Testing and Prescriptions for Urinary Stone Disease-Related Medications in VeteransShen Song, I-Chun Thomas, Calyani Ganesan, et al.
Nucleic Acids Research|March 24, 2017
ICF-specific DNMT3B dysfunction interferes with intragenic regulation of mRNA transcription and alternative splicingSole Gatto, Miriam Gagliardi, Monica Franzese, et al.
American Journal of Human Genetics|October 23, 1997
Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2M Horwitz, K F Benson, F Q Li, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Journal of Medical Genetics|June 5, 2010
Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancerDeborah W Neklason, Thérèse M Tuohy, Jeffery Stevens, et al.
Pageof 131