检索结果 - Liliane C. D. Wijnaendts
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Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene 由 Ronald H. Lekanne Deprez, J J Muurling-Vlietman, J Hruda, Marieke J.H. Baars, Liliane C. D. Wijnaendts, Irene Stolte‐Dijkstra, Mariëlle Alders, Johanna M. van Hagen
出版 2006Carta -
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PPIB Mutations Cause Severe Osteogenesis Imperfecta 由 Fleur S. van Dijk, I. M. Nesbitt, Eline H. Zwikstra, Peter G. J. Nikkels, Sander R. Piersma, Silvina A. Fratantoni, Connie R. Jiménez, Margriet Huizer, Alice C. Morsman, Jan M. Cobben, Mirjam H.H. van Roij, Mariet W. Elting, Jonathan Verbeke, Liliane C. D. Wijnaendts, Nick J. Shaw, Wolfgang Högler, C McKeown, Erik A. Sistermans, Ann Dalton, Hanne Meijers‐Heijboer, Gerard Pals
出版 2009Artigo
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Biology
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Hypertrophic cardiomyopathy