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Publications by S M Reamon-Buettner

Somatic NKX2-5 Mutations as a Novel Mechanism of Disease in Complex Congenital Heart Disease

Journal of Medical Genetics
Genetics
2004English

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Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

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Novel NKX2-5 Mutations Responsible for Congenital Heart Disease

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Novel PITX2c Loss-Of-Function Mutations Associated With Complex Congenital Heart Disease

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Advancing Prenatal Detection of Congenital Heart Disease: A Novel Screening Protocol Improves Early Diagnosis of Complex Congenital Heart Disease

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EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Prenatal Diagnosis of Congenital Heart Disease

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Fetal Somatic Growth Trajectory Differs by Type of Congenital Heart Disease

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Mechanism of Myocardial Microvessel Formation in Cyanotic Congenital Heart Disease

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Congenital Heart Disease

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2012English

Quality of Life in Surgically Palliated Complex Congenital Heart Disease.

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