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Katharina Schwan

Showing results (1-10 of 5) with videos related to

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Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|December 20, 2022
The maximum phonation time as marker for voice treatment efficacy: A network meta-analysisBen Barsties V Latoszek, Christopher R Watts, Katharina Schwan, et al.
International Journal of Neonatal Screening|October 19, 2020
Family Perspectives on Newborn Screening for X-Linked Adrenoleukodystrophy in CaliforniaKatharina Schwan, Janey Youngblom, Kara Weisiger, et al.
Journal of Graduate Medical Education|August 22, 2017
Doing More With Less: A Centralized Model for Fellowship Program CoordinationTwinkle Patel, Katharina Schwan, Sara Hoover, et al.
American Journal of Human Genetics|December 17, 2022
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
American Journal of Human Genetics|March 3, 2023
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|December 20, 2022
The maximum phonation time as marker for voice treatment efficacy: A network meta-analysisBen Barsties V Latoszek, Christopher R Watts, Katharina Schwan, et al.
International Journal of Neonatal Screening|October 19, 2020
Family Perspectives on Newborn Screening for X-Linked Adrenoleukodystrophy in CaliforniaKatharina Schwan, Janey Youngblom, Kara Weisiger, et al.
Journal of Graduate Medical Education|August 22, 2017
Doing More With Less: A Centralized Model for Fellowship Program CoordinationTwinkle Patel, Katharina Schwan, Sara Hoover, et al.
American Journal of Human Genetics|December 17, 2022
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
American Journal of Human Genetics|March 3, 2023
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsyMaimuna S Paul, Anna R Duncan, Casie A Genetti, et al.
Pageof 1