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David T Miller

Showing results (51-60 of 107) with videos related to

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Neonatology|October 19, 2016
Long-Gap Esophageal Atresia Is a Unique Entity within the Esophageal Atresia Defect SpectrumSigrid Bairdain, David Zurakowski, Sara O Vargas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2020
Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disabilityJennifer Malinowski, David T Miller, Laurie Demmer, et al.
Hypertension (Dallas, Tex. : 1979)|November 16, 2011
Mechanisms of premature vascular aging in children with Hutchinson-Gilford progeria syndromeMarie Gerhard-Herman, Leslie B Smoot, Nicole Wake, et al.
Pediatric Radiology|July 4, 2012
A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndromeRobert H Cleveland, Leslie B Gordon, Monica E Kleinman, et al.
The Journal of Allergy and Clinical Immunology|January 31, 2009
Novel presentation of Omenn syndrome in association with aniridiaWilliam J Sheehan, Ottavia M Delmonte, David T Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 12, 2019
Response to Knoppers et alKaren L David, Robert G Best, Leslie Manace Brenman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2018
Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG)Karen L David, Robert G Best, Leslie Manace Brenman, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 30, 2011
Hutchinson-Gilford progeria is a skeletal dysplasiaCatherine M Gordon, Leslie B Gordon, Brian D Snyder, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalitiesHeather Mason-Suares, Wayne Kim, Leslie Grimmett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Pageof 11

Showing results (51-60 of 107) with videos related to

Sort By:
Pageof 11
Neonatology|October 19, 2016
Long-Gap Esophageal Atresia Is a Unique Entity within the Esophageal Atresia Defect SpectrumSigrid Bairdain, David Zurakowski, Sara O Vargas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 24, 2020
Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disabilityJennifer Malinowski, David T Miller, Laurie Demmer, et al.
Hypertension (Dallas, Tex. : 1979)|November 16, 2011
Mechanisms of premature vascular aging in children with Hutchinson-Gilford progeria syndromeMarie Gerhard-Herman, Leslie B Smoot, Nicole Wake, et al.
Pediatric Radiology|July 4, 2012
A prospective study of radiographic manifestations in Hutchinson-Gilford progeria syndromeRobert H Cleveland, Leslie B Gordon, Monica E Kleinman, et al.
The Journal of Allergy and Clinical Immunology|January 31, 2009
Novel presentation of Omenn syndrome in association with aniridiaWilliam J Sheehan, Ottavia M Delmonte, David T Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 12, 2019
Response to Knoppers et alKaren L David, Robert G Best, Leslie Manace Brenman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2018
Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG)Karen L David, Robert G Best, Leslie Manace Brenman, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 30, 2011
Hutchinson-Gilford progeria is a skeletal dysplasiaCatherine M Gordon, Leslie B Gordon, Brian D Snyder, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2013
Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalitiesHeather Mason-Suares, Wayne Kim, Leslie Grimmett, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)Darrel Waggoner, Karen E Wain, Adrian M Dubuc, et al.
Pageof 11