Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="MEFFORD, HC" or (type any "bookEditor issueEditor" and editor="MEFFORD, HC") Add to list Journal Article A1 open access Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome BWM van Bon, HC Mefford, Björn Menten (UGent) , DA Koolen, AJ Sharp, WM Nillesen, JW Innis, TJL de Ravel, CL Mercer, M Fichera, et al. (2009) JOURNAL OF MEDICAL GENETICS. 46(8). p.511-523 Add to list Journal Article A1 Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes HC MEFFORD, AJ SHARP, C BAKER, A ITSARA, ZS JIANG, Karen Buysse (UGent) , SW HUANG, VK MALONEY, JA CROLLA, D BARALLE, et al. (2008) NEW ENGLAND JOURNAL OF MEDICINE. 359(16).