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Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities
Weterman, M. A. J., Kuo, M., Kenter, S. B., Gordillo, S., Karjosukarso, D. W., Takase, R., Bronk, M., Oprescu, S., van Ruissen, F., Witteveen, R. J. W., Bienfait, H. M. E., Breuning, M., Verhamme, C., Hou, Y.-M., de Visser, M., Antonellis, A. & Baas, F., 2018, In: Human molecular genetics. 27, 23, p. 4036-4050Research output: Contribution to journal › Article* › Academic › peer-review
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Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri
van den Munckhof, P., Christiaans, I., Kenter, S. B., Baas, F. & Hulsebos, T. J. M., 2012, In: Neurogenetics. 13, 1, p. 1-7Research output: Contribution to journal › Article* › Academic › peer-review
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Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas
Christiaans, I., Kenter, S. B., Brink, H. C., van Os, T. A. M., Baas, F., van den Munckhof, P., Kidd, A. M. J. & Hulsebos, T. J. M., 2011, In: Journal of medical genetics. 48, 2, p. 93-97Research output: Contribution to journal › Article* › Academic › peer-review
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