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Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal.
Postma AV, Alders M, Sylva M, Bilardo CM, Pajkrt E, van Rijn RR, Schulte-Merker S, Bulk S, Stefanovic S, Ilgun A, Barnett P, Mannens MM, Moorman AF, Oostra RJ, van Maarle MC. Postma AV, et al. Among authors: sylva m. J Med Genet. 2014 Feb;51(2):90-7. doi: 10.1136/jmedgenet-2013-102001. Epub 2013 Nov 19. J Med Genet. 2014. PMID: 24253444
Development of the human heart.
Sylva M, van den Hoff MJ, Moorman AF. Sylva M, et al. Am J Med Genet A. 2014 Jun;164A(6):1347-71. doi: 10.1002/ajmg.a.35896. Epub 2013 Apr 30. Am J Med Genet A. 2014. PMID: 23633400 Review.
Follistatin-like 1 in vertebrate development.
Sylva M, Moorman AF, van den Hoff MJ. Sylva M, et al. Birth Defects Res C Embryo Today. 2013 Mar;99(1):61-9. doi: 10.1002/bdrc.21030. Birth Defects Res C Embryo Today. 2013. PMID: 23723173 Review.
Renal expression of CD44 correlates with acute renal allograft rejection.
Rouschop KM, Roelofs JJ, Sylva M, Rowshani AT, Ten Berge IJ, Weening JJ, Florquin S. Rouschop KM, et al. Among authors: sylva m. Kidney Int. 2006 Sep;70(6):1127-34. doi: 10.1038/sj.ki.5001711. Epub 2006 Jul 26. Kidney Int. 2006. PMID: 16871244 Free article.
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