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Items: 4

1.

Acute pancreatitis complicated with choledochal duct rupture.

Bouvry M, Van Renterghem K, Verrijckt A, Smeets P, Meersschaut V, Vande Velde S, De Bruyne R, De Vos M, Van Winckel M, Van Biervliet S.

Case Rep Gastrointest Med. 2011;2011:413268. doi: 10.1155/2011/413268. Epub 2011 Oct 3.

2.

Genetic screening of LCA in Belgium: predominance of CEP290 and identification of potential modifier alleles in AHI1 of CEP290-related phenotypes.

Coppieters F, Casteels I, Meire F, De Jaegere S, Hooghe S, van Regemorter N, Van Esch H, Matuleviciene A, Nunes L, Meersschaut V, Walraedt S, Standaert L, Coucke P, Hoeben H, Kroes HY, Vande Walle J, de Ravel T, Leroy BP, De Baere E.

Hum Mutat. 2010 Oct;31(10):E1709-66. doi: 10.1002/humu.21336.

3.

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects.

Roels F, Verloo P, Eyskens F, Fran├žois B, Seneca S, De Paepe B, Martin JJ, Meersschaut V, Praet M, Scalais E, Espeel M, Smet J, Van Goethem G, Van Coster R.

BMC Clin Pathol. 2009 Jun 5;9:4. doi: 10.1186/1472-6890-9-4.

4.

Report of a female patient with mental retardation and tall stature due to a chromosomal rearrangement disrupting the OPHN1 gene on Xq12.

Menten B, Buysse K, Vermeulen S, Meersschaut V, Vandesompele J, Ng BL, Carter NP, Mortier GR, Speleman F.

Eur J Med Genet. 2007 Nov-Dec;50(6):446-54. Epub 2007 Aug 6.

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