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  1. 2019

  2. Identifying pathogenic variants in the Follistatin-like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disorders

    Prakash, S., Mattiotti, A., Sylva, M., Mulder, B. J. M., Postma, A. V. & van den Hoff, M. J. B., 2019, In: Molecular genetics and genomic medicine. 7, 4, e00567.

    Research output: Contribution to journal › Article › Academic › peer-review

  3. Severe fetal hemolysis and cholestasis due to high-titer maternal IgG anti-A antibodies

    Zonneveld, R., van der Meer-Kapelle, L., Sylva, M., Brand, A., Zijlstra, M. & Schonewille, H., 2019, In: Pediatrics. 143, 4, e20182859.

    Research output: Contribution to journal › Article › Academic › peer-review

  4. 2017

  5. Deletion of Fstl1 (Follistatin-Like 1) From the Endocardial/Endothelial Lineage Causes Mitral Valve Disease

    Prakash, S., Borreguero, L. J. J., Sylva, M., Flores Ruiz, L., Rezai, F., Gunst, Q. D., de la Pompa, J-L., Ruijter, J. M. & van den Hoff, M. J. B., 2017, In: Arteriosclerosis, thrombosis, and vascular biology. 37, 9, p. E116-E130

    Research output: Contribution to journal › Article › Academic › peer-review

  6. 2015

  7. Normal Development of the heart

    Sylva, M. & Moorman, A. F. M., 2015, Congenital Heart Disease. Muenke, M., Kruszka, P. S., Sable, C. A. & Belmont, J. W. (eds.). Houston, Texas: Karger, p. 11-24

    Research output: Chapter in Book/Report/Conference proceeding › Chapter › Academic › peer-review

  8. 2014

  9. Development of the human heart

    Sylva, M., van den Hoff, M. J. B. & Moorman, A. F. M., 2014, In: American journal of medical genetics. Part A. 164A, 6, p. 1347-1371

    Research output: Contribution to journal › Article › Academic › peer-review

  10. 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, A. V., Alders, M., Sylva, M., Bilardo, C. M., Pajkrt, E., van Rijn, R. R., Schulte-Merker, S., Bulk, S., Stefanovic, S., Ilgun, A., Barnett, P., Mannens, M. M. A. M., Moorman, A. F. M., Oostra, R. J. & van Maarle, M. C., 2014, In: Journal of medical genetics. 51, 2, p. 90-97

    Research output: Contribution to journal › Article › Academic › peer-review

  11. On the connective tissue regulator Follistatin-like 1

    Sylva, M., 2014, 184 p.

    Research output: PhD Thesis › Phd-Thesis - Research and graduation internal

  12. 2013

  13. Follistatin-like 1 in vertebrate development

    Sylva, M., Moorman, A. F. M. & van den Hoff, M. J. B., 2013, In: Birth defects research. Part C, Embryo today. 99, 1, p. 61-69

    Research output: Contribution to journal › Review article › Academic › peer-review

  14. Reduced sodium channel function unmasks residual embryonic slow conduction in the adult right ventricular outflow tract

    Boukens, B. J., Sylva, M., de Gier-de Vries, C., Remme, C. A., Bezzina, C. R., Christoffels, V. M. & Coronel, R., 2013, In: Circulation research. 113, 2, p. 137-141

    Research output: Contribution to journal › Article › Academic › peer-review

  15. 2011

  16. The BMP antagonist follistatin-like 1 is required for skeletal and lung organogenesis

    Sylva, M., Li, V. S. W., Buffing, A. A. A., van Es, J. H., van den Born, M., van der Velden, S., Gunst, Q., Koolstra, J. H., Moorman, A. F. M., Clevers, H. & van den Hoff, M. J. B., 2011, In: PLoS ONE. 6, 8, p. e22616

    Research output: Contribution to journal › Article › Academic › peer-review

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