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Maternal experience of fetal movements from a child with AMC: MECA survey
Arduç, A., Linskens, I. H., Dussa, C. U., van Bosse, H., Lemin, S., Sawatzky, B. & the MECA Study Group, 1 Aug 2025, In: Early Human Development. 207, 106308.Research output: Contribution to journal › Article* › Academic › peer-review
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Human Phenotype Ontology Annotations for Rare Congenital Conditions: Application to Arthrogryposis Multiplex Congenita
Nematollahi, S., Hamdy, R. C., van Bosse, H., Li, J., Blanshay-Goldberg, D., de Vries, J. I. P., Dieterich, K., Filges, I., Bedard, T., Haendel, M., Torres, M. M., Robinson, P. N. & Dahan-Oliel, N., Aug 2025, In: American Journal of Medical Genetics. Part A. 197, 8, e64067.Research output: Contribution to journal › Article* › Academic › peer-review
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Perinatal genetic diagnostic yield in a population of fetuses with the phenotype arthrogryposis multiplex congenita: a cohort study 2007–2021
Arduç, A., de Vries, J. I. P., B. Tan-Sindhunata, M., Waisfisz, Q., Pajkrt, E. & Linskens, I. H., 2025, (E-pub ahead of print) In: European journal of human genetics. 148.Research output: Contribution to journal › Article* › Academic › peer-review
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