A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p

M.W. Wessels, B.M. de Graaf, T.E. Cohen-Overbeek, S.E. Spitaels, L. de Groot-de Laat, F.J. ten Cate, I.F.M. Frohn-Mulder, R. de Krijger, M.M. Bartelings, N. Essed, J.W. Wladimiroff, M.F. Niermeijer, P. Heutink, B.A. Oostra, D. Dooijes, A.M. Bertoli-Avella, P.J. Willems

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)595-603
JournalHuman Genetics
Volume122
Issue number6
DOIs
Publication statusPublished - 2008

Cite this

Wessels, M. W., de Graaf, B. M., Cohen-Overbeek, T. E., Spitaels, S. E., de Groot-de Laat, L., ten Cate, F. J., ... Willems, P. J. (2008). A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p. Human Genetics, 122(6), 595-603. https://doi.org/10.1007/s00439-007-0436-x