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Dive into the research topics of 'A familial congenital heart disease with a possible multigenic origin involving a mutation in BMPR1A'. Together they form a unique fingerprint.- Sort by
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Till Joscha Demal, Melina Heise, Benedikt Reiz, Deepika Dogra, Ingrid Brænne, Hermann Reichenspurner, Jörg Männer, Zouhair Aherrahrou, Heribert Schunkert, Jeanette Erdmann*, Salim Abdelilah-Seyfried