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Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.
Am J Med Genet A. 2013 Dec;161A(12):3187-90. doi: 10.1002/ajmg.a.36182. Epub 2013 Aug 16.
Am J Med Genet A. 2013.
PMID: 23956225
Hemophagocytic lymphohistiocytosis in a patient with deletion of 22q11.2.
Aricò M, Bettinelli A, Maccario R, Clementi R, Bossi G, Danesino C.
Aricò M, et al.
Am J Med Genet. 1999 Dec 3;87(4):329-30.
Am J Med Genet. 1999.
PMID: 10588839
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