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Steven B Bleyl

Showing results (11-20 of 44) with videos related to

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Developmental Biology|June 14, 2011
Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular developmentLisa D Urness, Steven B Bleyl, Tracy J Wright, et al.
Pediatric Blood & Cancer|September 18, 2010
Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous systemCarol S Bruggers, Steven B Bleyl, Theodore Pysher, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 13, 2017
Use of Extracorporeal Membrane Oxygenation and Mortality in Pediatric Cardiac Surgery Patients With Genetic Conditions: A Multicenter AnalysisJamie M Furlong-Dillard, Venugopal Amula, David K Bailly, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Phenotype of a patient with contiguous deletion of TBX5 and TBX3: expanding the disease spectrumSoujanya Bogarapu, Steven B Bleyl, Amy Calhoun, et al.
Cardiology in the Young|May 17, 2018
DMD mutation and LTBP4 haplotype do not predict onset of left ventricular dysfunction in Duchenne muscular dystrophyCharlotte S Van Dorn, Michael D Puchalski, Hsin-Yi Weng, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Analysis of a Scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12Steven B Bleyl, Lorenzo D Botto, John C Carey, et al.
American Journal of Medical Genetics. Part A|February 19, 2019
Expanding the genetic and clinical spectrum of the NONO-associated X-linked intellectual disability syndromeColleen M Carlston, Steven B Bleyl, Ashley Andrews, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2021
A qualitative study of prevalent laboratory information systems and data communication patterns for genetic test reportingAly Khalifa, Clinton C Mason, Jennifer Hornung Garvin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2021
A qualitative investigation of biomedical informatics interoperability standards for genetic test reporting: benefits, challenges, and motivations from the testing laboratory's perspectiveAly Khalifa, Clinton C Mason, Jennifer Hornung Garvin, et al.
Journal of the American Medical Informatics Association : JAMIA|September 27, 2021
Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelinesAly Khalifa, Clinton C Mason, Jennifer Hornung Garvin, et al.
Pageof 5

Showing results (11-20 of 44) with videos related to

Sort By:
Pageof 5
Developmental Biology|June 14, 2011
Redundant and dosage sensitive requirements for Fgf3 and Fgf10 in cardiovascular developmentLisa D Urness, Steven B Bleyl, Tracy J Wright, et al.
Pediatric Blood & Cancer|September 18, 2010
Clinicopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous systemCarol S Bruggers, Steven B Bleyl, Theodore Pysher, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 13, 2017
Use of Extracorporeal Membrane Oxygenation and Mortality in Pediatric Cardiac Surgery Patients With Genetic Conditions: A Multicenter AnalysisJamie M Furlong-Dillard, Venugopal Amula, David K Bailly, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Phenotype of a patient with contiguous deletion of TBX5 and TBX3: expanding the disease spectrumSoujanya Bogarapu, Steven B Bleyl, Amy Calhoun, et al.
Cardiology in the Young|May 17, 2018
DMD mutation and LTBP4 haplotype do not predict onset of left ventricular dysfunction in Duchenne muscular dystrophyCharlotte S Van Dorn, Michael D Puchalski, Hsin-Yi Weng, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Analysis of a Scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12Steven B Bleyl, Lorenzo D Botto, John C Carey, et al.
American Journal of Medical Genetics. Part A|February 19, 2019
Expanding the genetic and clinical spectrum of the NONO-associated X-linked intellectual disability syndromeColleen M Carlston, Steven B Bleyl, Ashley Andrews, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2021
A qualitative study of prevalent laboratory information systems and data communication patterns for genetic test reportingAly Khalifa, Clinton C Mason, Jennifer Hornung Garvin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 25, 2021
A qualitative investigation of biomedical informatics interoperability standards for genetic test reporting: benefits, challenges, and motivations from the testing laboratory's perspectiveAly Khalifa, Clinton C Mason, Jennifer Hornung Garvin, et al.
Journal of the American Medical Informatics Association : JAMIA|September 27, 2021
Interoperable genetic lab test reports: mapping key data elements to HL7 FHIR specifications and professional reporting guidelinesAly Khalifa, Clinton C Mason, Jennifer Hornung Garvin, et al.
Pageof 5