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Tara L Wenger

Showing results (1-10 of 46) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 18, 2024
A plot TWISTSophia R Meyer, Tara L Wenger
The Journal of Pediatrics|March 19, 2018
Delayed Subaponeurotic Fluid Collections of InfancyJonathan J Lee, Tara L Wenger
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 15, 2025
Commentary: Interventional GeneticsTara L Wenger, Margaret P Adam
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 31, 2025
Treatment of PDGFRB-Related Penttinen Syndrome With Imatinib in a Young ChildMolly McPheron, Katelyn Burns, Tara L Wenger
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 12, 2018
An Algorithm for the Assessment of Facial Asymmetry in Children With Focus on Etiology and TreatmentTara L Wenger, Emily R Gallagher, Elizabeth J Bhoj
The Journal of Pediatrics|June 13, 2016
Role of Pediatric Geneticists in Craniofacial Teams: The Identification of Craniofacial Conditions with Cancer PredispositionTara L Wenger, Dawn Earl, Penny Chow, et al.
American Journal of Medical Genetics. Part A|January 12, 2021
41st Annual David W. Smith workshop on malformations and morphogenesis: Abstracts of the 2020 annual meetingKaren W Gripp, Kenneth Lyons Jones, Tara L Wenger, et al.
American Journal of Medical Genetics. Part A|December 14, 2019
Catel-Manzke syndrome without Manzke dysostosisDanny E Miller, Penny Chow, Emily R Gallagher, et al.
Neurosurgical Focus|November 2, 2016
Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhageHannah M Tully, Tara L Wenger, Walter A Kukull, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortalityTara L Wenger, Richard A Hopper, Anna Rosen, et al.
Pageof 5

Showing results (1-10 of 46) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|June 18, 2024
A plot TWISTSophia R Meyer, Tara L Wenger
The Journal of Pediatrics|March 19, 2018
Delayed Subaponeurotic Fluid Collections of InfancyJonathan J Lee, Tara L Wenger
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|September 15, 2025
Commentary: Interventional GeneticsTara L Wenger, Margaret P Adam
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 31, 2025
Treatment of PDGFRB-Related Penttinen Syndrome With Imatinib in a Young ChildMolly McPheron, Katelyn Burns, Tara L Wenger
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 12, 2018
An Algorithm for the Assessment of Facial Asymmetry in Children With Focus on Etiology and TreatmentTara L Wenger, Emily R Gallagher, Elizabeth J Bhoj
The Journal of Pediatrics|June 13, 2016
Role of Pediatric Geneticists in Craniofacial Teams: The Identification of Craniofacial Conditions with Cancer PredispositionTara L Wenger, Dawn Earl, Penny Chow, et al.
American Journal of Medical Genetics. Part A|January 12, 2021
41st Annual David W. Smith workshop on malformations and morphogenesis: Abstracts of the 2020 annual meetingKaren W Gripp, Kenneth Lyons Jones, Tara L Wenger, et al.
American Journal of Medical Genetics. Part A|December 14, 2019
Catel-Manzke syndrome without Manzke dysostosisDanny E Miller, Penny Chow, Emily R Gallagher, et al.
Neurosurgical Focus|November 2, 2016
Anatomical configurations associated with posthemorrhagic hydrocephalus among premature infants with intraventricular hemorrhageHannah M Tully, Tara L Wenger, Walter A Kukull, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 20, 2018
A genotype-specific surgical approach for patients with Pfeiffer syndrome due to W290C pathogenic variant in FGFR2 is associated with improved developmental outcomes and reduced mortalityTara L Wenger, Richard A Hopper, Anna Rosen, et al.
Pageof 5