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- Systematic Detection of Brain Protein-Coding Genes Under Positive Selection During Primate Evolution and Their Roles in Cognition
- Loss-Of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects
- Primary Ciliary Dyskinesia
- Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
- 1 TITLE (146 Characters) AUTHORS Ignasi Sahún1,*, Damien Marechal2,3,4,5*, Patricia Lopes Pereira2,§, Valérie Nalesso2
- Primary Ciliary Dyskinesia, a Motile Cilia Disorder Kavita Praveen, Erica E
- Mucociliary Respiratory Epithelium Integrity in Molecular Defense and Susceptibility to Pulmonary Viral Infections
- Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease
- Zebrafish Motile Cilia As a Model for Primary Ciliary Dyskinesia
- Primary Ciliary Dyskinesia Panel
- Ciliopathies Gene Panel
- Newborndxtm Advanced Sequencing Evaluation Disorders List
- Identifying Novel Genetic Causes of Primary Ciliary Dyskinesia
- Supplimentry Figure 1- GSEA Plot of All the Significantly Enriched Data Sets
- Mackenzie's Mission Gene & Condition List
- Cone Rod Dystrophy Precision Panel Overview Indications Clinical Utility
- Genomic Copy Number Variation in Mus Musculus
- Molecular Testing by Next Generation Sequencing for Mutations Associated with Primary Ciliary Dyskinesia / Kartagener Syndrome