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Showing results (21-30 of 70) with videos related to

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Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|January 30, 2023
Genetic heterogeneity and enrichment of variants in DNA-repair genes in ameloblastomaWaheed Awotoye, Joseph Craig Whitt, Byunggil Yoo, et al.
Genome Medicine|March 31, 2012
Next-generation community genetics for low- and middle-income countriesStephen F Kingsmore, John D Lantos, Darrell L Dinwiddie, et al.
BMC Medical Genomics|September 19, 2013
De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomaliesDarrell L Dinwiddie, Sarah E Soden, Carol J Saunders, et al.
Mutation Research|May 1, 1982
An evaluation of the host-mediated assay and body fluid analysis. A report of the U.S. Environmental Protection Agency Gene-Tox ProgramM S Legator, E Bueding, R Batzinger, et al.
Journal of Neurosurgery|September 15, 2009
True posterior communicating artery aneurysms: are they more prone to rupture? A biomorphometric analysisWenzhuan He, Jason Hauptman, Latha Pasupuleti, et al.
Nature|January 22, 2025
Rapid and scalable personalized ASO screening in patient-derived organoidsJohn C Means, Anabel L Martinez-Bengochea, Daniel A Louiselle, et al.
Nature Communications|January 22, 2024
Pangenome graphs improve the analysis of structural variants in rare genetic diseasesCristian Groza, Carl Schwendinger-Schreck, Warren A Cheung, et al.
Genomics|May 2, 2013
Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genomeDarrell L Dinwiddie, Laurie D Smith, Neil A Miller, et al.
American Journal of Physiology. Endocrinology and Metabolism|August 7, 2008
Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosisHolly J Garringer, Mahdi Malekpour, Fatemehsadat Esteghamat, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|January 30, 2023
Genetic heterogeneity and enrichment of variants in DNA-repair genes in ameloblastomaWaheed Awotoye, Joseph Craig Whitt, Byunggil Yoo, et al.
Genome Medicine|March 31, 2012
Next-generation community genetics for low- and middle-income countriesStephen F Kingsmore, John D Lantos, Darrell L Dinwiddie, et al.
BMC Medical Genomics|September 19, 2013
De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomaliesDarrell L Dinwiddie, Sarah E Soden, Carol J Saunders, et al.
Mutation Research|May 1, 1982
An evaluation of the host-mediated assay and body fluid analysis. A report of the U.S. Environmental Protection Agency Gene-Tox ProgramM S Legator, E Bueding, R Batzinger, et al.
Journal of Neurosurgery|September 15, 2009
True posterior communicating artery aneurysms: are they more prone to rupture? A biomorphometric analysisWenzhuan He, Jason Hauptman, Latha Pasupuleti, et al.
Nature|January 22, 2025
Rapid and scalable personalized ASO screening in patient-derived organoidsJohn C Means, Anabel L Martinez-Bengochea, Daniel A Louiselle, et al.
Nature Communications|January 22, 2024
Pangenome graphs improve the analysis of structural variants in rare genetic diseasesCristian Groza, Carl Schwendinger-Schreck, Warren A Cheung, et al.
Genomics|May 2, 2013
Diagnosis of mitochondrial disorders by concomitant next-generation sequencing of the exome and mitochondrial genomeDarrell L Dinwiddie, Laurie D Smith, Neil A Miller, et al.
American Journal of Physiology. Endocrinology and Metabolism|August 7, 2008
Molecular genetic and biochemical analyses of FGF23 mutations in familial tumoral calcinosisHolly J Garringer, Mahdi Malekpour, Fatemehsadat Esteghamat, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|November 5, 2008
A case of familial tumoral calcinosis/hyperostosis-hyperphosphatemia syndrome due to a compound heterozygous mutation in GALNT3 demonstrating new phenotypic featuresC E Dumitrescu, M H Kelly, A Khosravi, et al.
Pageof 7