| scholarly article | Q13442814 |
| P2093 | author name string | J Goodship | |
| A F M Moorman | |||
| T Rahman | |||
| U Bauer | |||
| B J M Mulder | |||
| H W Vliegen | |||
| J W Roos-Hesselink | |||
| T Pickardt | |||
| A V Postma | |||
| A T J M Helderman-van den Enden | |||
| B Keavney | |||
| J B A van de Meerakker | |||
| J-W Sels | |||
| K van Engelen | |||
| M J H Baars | |||
| S Klaassen | |||
| S R Sperling | |||
| P2860 | cites work | ??? | Q28304085 |
| Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways | Q22010903 | ||
| Mutation in myosin heavy chain 6 causes atrial septal defect | Q24296801 | ||
| α-cardiac actin mutations produce atrial septal defects | Q24298075 | ||
| Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus | Q24302408 | ||
| Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects | Q24316985 | ||
| Mutations in sarcomere protein genes in left ventricular noncompaction | Q28281620 | ||
| Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene | Q33312381 | ||
| Morphological aspects of Ebstein's anomaly in adults | Q34045713 | ||
| Clinical features of isolated ventricular noncompaction in adults long-term clinical course, echocardiographic properties, and predictors of left ventricular failure | Q34573379 | ||
| Ebstein's anomaly | Q34602797 | ||
| Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation | Q34615184 | ||
| Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections. | Q34712315 | ||
| Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy | Q35382044 | ||
| Oriented clonal cell growth in the developing mouse myocardium underlies cardiac morphogenesis | Q36321793 | ||
| Analysis of ventricular hypertrabeculation and noncompaction using genetically engineered mouse models | Q37352201 | ||
| Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases | Q37786123 | ||
| Ebstein's anomaly and extracardiac defects | Q38836973 | ||
| Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene | Q43145730 | ||
| Lineage and morphogenetic analysis of the cardiac valves. | Q44228444 | ||
| Ebstein's malformation of the tricuspid valve: genetic and environmental factors. The Baltimore-Washington Infant Study Group | Q46097400 | ||
| Left heart lesions in patients with Ebstein anomaly. | Q47878221 | ||
| Noncompacted myocardium in Ebstein's anomaly: initial description in three patients | Q47880745 | ||
| Familial biventricular myocardial noncompaction associated with Ebstein's malformation. | Q52045962 | ||
| The Importance of Genetic Counseling, DNA Diagnostics, and Cardiologic Family Screening in Left Ventricular Noncompaction Cardiomyopathy | Q57364826 | ||
| Ebstein Anomaly Associated With Left Ventricular Noncompaction | Q57785553 | ||
| Mutations in the Sarcomere Gene MYH7 in Ebstein Anomaly | Q61650582 | ||
| Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis | Q74137278 | ||
| A rare case of interstitial del(1)(p34.3p36.11) diagnosed prenatally | Q81046909 | ||
| Ebstein anomaly and duplication of the distal arm of chromosome 15: report of two patients | Q81461447 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 113-117 | |
| P577 | publication date | 2013-03-01 | |
| P1433 | published in | Netherlands Heart Journal | Q2146163 |
| P1476 | title | Ebstein's anomaly may be caused by mutations in the sarcomere protein gene MYH7. | |
| P478 | volume | 21 |
| Q26748789 | A Biobank for Long-term and Sustainable Research in the Field of Congenital Heart Disease in Germany |
| Q41836007 | A patient of Ebstein's anomaly associated with biventricular noncompaction presented with Wolf Parkinson White syndrome - A rare presentation |
| Q48101181 | Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO. |
| Q38116488 | Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7. |
| Q36185458 | Human gene copy number spectra analysis in congenital heart malformations |
| Q40573732 | Incidental Finding of Ebstein's Anomaly in an Adolescent with an Upper Respiratory Infection: A Case Report |
| Q44209295 | Perinatal course of Ebstein's anomaly and tricuspid valve dysplasia in the fetus |
| Q38240077 | Structural implications of β-cardiac myosin heavy chain mutations in human disease |
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