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Additional file 4: Figure S4. of Methylome analysis for spina bifida shows SOX18 hypomethylation as a risk factor with evidence for a complex (epi)genetic interplay to affect neural tube development

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posted on 13.10.2016, 05:00 authored by Anne Rochtus, Raf Winand, Griet Laenen, Elise Vangeel, Benedetta Izzi, Christine Wittevrongel, Yves Moreau, Carla Verpoorten, Katrien Jansen, Chris Van Geet, Kathleen Freson
Genetic deletion on Chr 14q22 of Caucasian boy with lumbosacral myelomeningocele. Bar indicates 1.665-kb deletion on chromosome 14q22.1q22.2 (53,267,987-54,933,219) encompassing the genes FERMT2, DDHD1, BMP4, DKN3, and CNIH. Nucleotide positions accord to NCBI build 37/hg19. (PDF 9 kb)


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