Left-ventricular non-compaction (LVNC): A clinical feature more often observed in terminal deletion 1p36 than previously expected

Author:

Cremer Kirsten,Lüdecke Hermann-Josef,Ruhr Frauke,Wieczorek Dagmar

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference10 articles.

1. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

2. 1p deletion syndrome: further clinical characterization of a common, important and often missed cause of developmental delay/mental retardation;Battaglia;Proc Greenwood Genet Center,2004

3. L.L. Brailey, C.M. Powell, J.C. Carey, Noncompaction of the ventricular myocardium in patients with 1p36 deletion [abstract]. Programme and Abstracts of the American College of Medical Genetics Annual Clinical Meeting; 23–26 March 2006; San Diego, CA: American College of Medical Genetics: 2006.

4. Monosomy 1p36 deletion syndrome;Gajecka;Am J Med Genet Part C Semin Med Genet,2007

5. Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality;Heilstedt;Clin Genet,2003

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