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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 29, 2011
Next generation massively parallel sequencing of targeted exomes to identify genetic mutations in primary ciliary dyskinesia: implications for application to clinical testingJonathan S Berg, James P Evans, Margaret W Leigh, et al.
Proteomics|July 23, 2003
Multiplex proteomic analysis by two-dimensional differential in-gel electrophoresisMichael R Knowles, Sandra Cervino, Heather A Skynner, et al.
Journal of Clinical Immunology|March 27, 2019
Nasal Nitric Oxide in Primary Immunodeficiency and Primary Ciliary Dyskinesia: Helping to Distinguish Between Clinically Similar DiseasesZofia N Zysman-Colman, Kimberley R Kaspy, Reza Alizadehfar, et al.
Pediatric Pulmonology|February 5, 2022
Going beyond the chest X-ray: Investigating laterality defects in primary ciliary dyskinesiaWallace B Wee, Kimberley R Kaspy, Michael G Sawras, et al.
The Journal of Pediatrics|July 29, 2014
Cri du chat syndrome and primary ciliary dyskinesia: a common genetic cause on chromosome 5pAdam J Shapiro, Karen E Weck, Kay C Chao, et al.
The American Journal of Gastroenterology|August 17, 2004
Analysis of cystic fibrosis gener product (CFTR) function in patients with pancreas divisum and recurrent acute pancreatitisAndres Gelrud, Sunil Sheth, Subhas Banerjee, et al.
Molecular Biology of the Cell|April 14, 2021
Structural insights into the cause of human RSPH4A primary ciliary dyskinesiaYanhe Zhao, Justine Pinskey, Jianfeng Lin, et al.
The European Respiratory Journal|May 16, 2015
A quality-of-life measure for adults with primary ciliary dyskinesia: QOL-PCDJane S Lucas, Laura Behan, Audrey Dunn Galvin, et al.
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