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C Brewer

Showing results (431-440 of 533) with videos related to

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Journal of Medical Genetics|February 4, 2005
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entitiesS P Pryor, A C Madeo, J C Reynolds, et al.
Journal of Religion and Health|July 12, 2018
Health Behaviors and Preventive Healthcare Utilization Among African-American Attendees at a Faith-Based Public Health Conference: Healthy Churches 2020Christopher T Pullins, Pernessa C Seele, Richard O White, et al.
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|December 16, 2019
Race and Gender Differences in Awareness of Colorectal Cancer Screening Tests and Guidelines Among Recently Diagnosed Colon Cancer Patients in an Urban SettingLeslie R Carnahan, Lindsey Jones, Katherine C Brewer, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Molecular Psychiatry|August 30, 2001
Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithiumG Turecki, P Grof, E Grof, et al.
Current Atherosclerosis Reports|June 15, 2026
Primary Prevention of Dyslipidemia: 10 Practice-Changing Takeaways from the 2026 ACC/AHA Multisociety GuidelineDmitry Abramov, Abdul Mannan Khan Minhas, Michael D Shapiro, et al.
The Journal of Clinical Endocrinology and Metabolism|October 25, 2012
Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excessAlison M Boyce, McKinley Glover, Marilyn H Kelly, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The Laryngoscope|December 30, 2022
Audiometric and Otologic Findings in Children and Young Adults with Neurofibromatosis Type 1 and Plexiform NeurofibromasVictoria Idowu, Julie Christensen, Andrea M Gross, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 6, 2009
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type CNicole M Yanjanin, Jorge I Vélez, Andrea Gropman, et al.
Pageof 54

Showing results (431-440 of 533) with videos related to

Sort By:
Pageof 54
Journal of Medical Genetics|February 4, 2005
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entitiesS P Pryor, A C Madeo, J C Reynolds, et al.
Journal of Religion and Health|July 12, 2018
Health Behaviors and Preventive Healthcare Utilization Among African-American Attendees at a Faith-Based Public Health Conference: Healthy Churches 2020Christopher T Pullins, Pernessa C Seele, Richard O White, et al.
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|December 16, 2019
Race and Gender Differences in Awareness of Colorectal Cancer Screening Tests and Guidelines Among Recently Diagnosed Colon Cancer Patients in an Urban SettingLeslie R Carnahan, Lindsey Jones, Katherine C Brewer, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Molecular Psychiatry|August 30, 2001
Mapping susceptibility genes for bipolar disorder: a pharmacogenetic approach based on excellent response to lithiumG Turecki, P Grof, E Grof, et al.
Current Atherosclerosis Reports|June 15, 2026
Primary Prevention of Dyslipidemia: 10 Practice-Changing Takeaways from the 2026 ACC/AHA Multisociety GuidelineDmitry Abramov, Abdul Mannan Khan Minhas, Michael D Shapiro, et al.
The Journal of Clinical Endocrinology and Metabolism|October 25, 2012
Optic neuropathy in McCune-Albright syndrome: effects of early diagnosis and treatment of growth hormone excessAlison M Boyce, McKinley Glover, Marilyn H Kelly, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The Laryngoscope|December 30, 2022
Audiometric and Otologic Findings in Children and Young Adults with Neurofibromatosis Type 1 and Plexiform NeurofibromasVictoria Idowu, Julie Christensen, Andrea M Gross, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 6, 2009
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type CNicole M Yanjanin, Jorge I Vélez, Andrea Gropman, et al.
Pageof 54