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Emily G Farrow

Showing results (11-20 of 58) 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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 31, 2019
Using dried blood spots for variant analysis for patients with haemophiliaLauren E Amos, Byunggil Yoo, Neil Miller, 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.
The Journal of Allergy and Clinical Immunology|December 4, 2015
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitisGiuliana Giardino, Vera Gallo, Domenico Somma, 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.
American Journal of Human Genetics|April 18, 2024
Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populationsAna S A Cohen, Courtney D Berrios, Tricia N Zion, et al.
Pageof 6

Showing results (11-20 of 58) with videos related to

Sort By:
Pageof 6
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.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 31, 2019
Using dried blood spots for variant analysis for patients with haemophiliaLauren E Amos, Byunggil Yoo, Neil Miller, 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.
The Journal of Allergy and Clinical Immunology|December 4, 2015
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitisGiuliana Giardino, Vera Gallo, Domenico Somma, 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.
American Journal of Human Genetics|April 18, 2024
Genomic Answers for Kids: Toward more equitable access to genomic testing for rare diseases in rural populationsAna S A Cohen, Courtney D Berrios, Tricia N Zion, et al.
Pageof 6