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

Marja W. Wessels; Bianca M. De Graaf; Titia E. Cohen-Overbeek; Silja E. Spitaels; Lotte E. de Groot-de Laat; Folkert J. Ten Cate; Ingrid F. M. Frohn-Mulder; Ronald de Krijger; Margot M. Bartelings; Nienke Essed; Jury W. Wladimiroff; Martinus F. Niermeijer; Peter Heutink; Ben A. Oostra; Dennis Dooijes; Aida M. Bertoli-Avella; Patrick J. Willems
Human Genetics · Vol. 122, Issue 6 · pp. 595-603 · 2008
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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2008-01-01
Publication Year2008
Volume122
Issue6
Pages595-603
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-007-0436-x

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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