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Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy.
Coppieters F, Van Schil K, Bauwens M, Verdin H, De Jaegher A, Syx D, Sante T, Lefever S, Abdelmoula NB, Depasse F, Casteels I, de Ravel T, Meire F, Leroy BP, De Baere E. Coppieters F, et al. Among authors: de jaegher a. Genet Med. 2014 Sep;16(9):671-80. doi: 10.1038/gim.2014.24. Epub 2014 Mar 13. Genet Med. 2014. PMID: 24625443 Free article.
Multiple magnet ingestion: a real challenge for the paediatric surgeon.
Van Biervliet S, Van de Putte D, De Jaegher A, Vande Velde S, De Bruyne R, Van Winckel M, Van Renterghem K. Van Biervliet S, et al. Among authors: de jaegher a. Acta Clin Belg. 2012 Jul-Aug;67(4):298-300. doi: 10.2143/ACB.67.4.2062677. Acta Clin Belg. 2012. PMID: 23019808