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dextrocardia
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Genetic Markers
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Most Correlated SNPs
DNAI1
DNAH5
DNAH11
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
determination of bilateral symmetry
ATP-dependent microtubule motor activity
dynein complex
pattern specification process
CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_2
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Mouse Phenotypes - Immotile cilia syndrome
OMIM - Congenital disorder
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Most Relevant Literature
BMP2 is a potential causative gene for isolated dextrocardia situs solitus.
Dextrocardia with pulmonary hypoplasia: an unusual cause of unilateral lung white-out.
Assessment of Myocardial Viability Using Nuclear Medicine Imaging in Dextrocardia.
Myocardial perfusion imaging performed by dedicated cardiac cadmium-zinc-telluride camera in dextroc…
Coronary Artery Bypass Grafting in a Patient With Multivessel Disease and Dextrocardia With Situs In…
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Optimal Insertion Depth of Left Internal Jugular Vein Catheter in Infants
Comparison of Carotid Peak Systolic Velocity Variation With Aortic Peak Systolic Velocity Variation …
Clinical Evaluation of the CM-1500 in Postoperative Surgery Patients
Evaluation of Physiological Variables and Detection of Blood Loss Using the Zynex Fluid Monitoring S…
Clinical Evaluation of the CM-1500 During Apheresis Blood Donation
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