20 results on '"Basson, Craig T."'
Search Results
2. A KCNE2 mutation in a patient with cardiac arrhythmia induced by auditory stimuli and serum electrolyte imbalance
3. Structural and Functional Genetic Disorders of the Great Vessels and Outflow Tracts
4. Haploinsufficiency at the Protein Kinase A RIα Gene Locus Leads to Fertility Defects in Male Mice and Men
5. Taking a bite out of hypertrophic cardiomyopathy: soy diet and disease
6. Update: PGD and Holt-Oram syndrome
7. The Carney Complex: Unusual Skin Findings and Recurrent Cardiac Myxoma
8. Mutation of Perinatal Myosin Heavy Chain
9. Rescue of Cardiac Defects in Id Knockout Embryos by Injection of Embryonic Stem Cells
10. Mutation of Perinatal Myosin Heavy Chain Associated with a Carney Complex Variant
11. Sparking the Failing Heart
12. High-Risk Patients with Ventricular Preexcitation - A Pendulum in Motion
13. Weekly Clinicopathological Exercises: Case 11-2002: A 27-Year-Old Woman with Two Intracardiac Masses and a History of Endocrinopathy
14. The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): Results from phase I and scientific opportunities in phase II
15. A Molecular Basis for Wolff-Parkinson-White Syndrome
16. Do Statins Afford Neuroprotection in Patients with Cerebral Ischaemia and Stroke?
17. Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complex
18. Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5
19. Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome Maps to a Locus on Chromosome 7q3
20. The Clinical And Genetic Spectrum Of The Holt-Oram Syndrome (Heart-Hand Syndrome)
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.