Showing results (571-580 of 778) with videos related to

Sort By:
Pageof 78
Ultrastructural Pathology|August 21, 2013
A new tool improves diagnostic test performance for transmission em evaluation of axonemal dynein armsW Keith Funkhouser, Marc Niethammer, Johnny L Carson, et al.
Nature Communications|December 5, 2014
Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesiaJianfeng Lin, Weining Yin, Maria C Smith, et al.
Molecular Genetics & Genomic Medicine|August 3, 2019
The expanding phenotype of OFD1-related disorders: Hemizygous loss-of-function variants in three patients with primary ciliary dyskinesiaWilliam B Hannah, Suzanne DeBrosse, BreAnna Kinghorn, et al.
Children (Basel, Switzerland)|July 2, 2021
Foundational Movement Skills and Play Behaviors during Recess among Preschool Children: A Compositional AnalysisLawrence Foweather, Matteo Crotti, Jonathan D Foulkes, et al.
Molecular Genetics & Genomic Medicine|June 16, 2021
Autosomal dominant variants in FOXJ1 causing primary ciliary dyskinesia in two patients with obstructive hydrocephalusAdam J Shapiro, Kimberley Kaspy, M Leigh Ann Daniels, et al.
The Journal of Pediatrics|May 15, 1998
Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurementsD C Wilson, L Ellis, J Zielenski, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 17, 2009
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndromeMargaret W Leigh, Jessica E Pittman, Johnny L Carson, et al.
Pageof 78