Works matching IS 15524868 AND DT 2013 AND VI 163C AND IP 3
Results: 8
Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 178, doi. 10.1002/ajmg.c.31365
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- Article
Embryonic cardiac chamber maturation: Trabeculation, conduction, and cardiomyocyte proliferation.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 157, doi. 10.1002/ajmg.c.31366
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- Article
Noncompaction in the fetus and neonate: An autopsy study.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 169, doi. 10.1002/ajmg.c.31367
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- Article
Arrhythmogenic right ventricular cardiomyopathy/Dysplasia (ARVC/D).
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 185, doi. 10.1002/ajmg.c.31368
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- Article
Molecular mechanism of ventricular trabeculation/compaction and the pathogenesis of the left ventricular noncompaction cardiomyopathy (LVNC).
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 144, doi. 10.1002/ajmg.c.31369
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- Article
Disorders of left ventricular trabeculation/compaction or right ventricular wall formation.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 141, doi. 10.1002/ajmg.c.31370
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- Article
Implications of genetic testing in noncompaction/hypertrabeculation.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 206, doi. 10.1002/ajmg.c.31371
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- Article
Barth syndrome.
- Published in:
- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 198, doi. 10.1002/ajmg.c.31372
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- Article