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van de Putte R, Dworschak GC, Brosens E, et al. A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Front Pediatr. 2020;8:310doi: 10.3389/fped.2020.00310.
van de Putte, R., Dworschak, G. C., Brosens, E., Reutter, H. M., Marcelis, C. L. M., Acuna-Hidalgo, R., Kurtas, N. E., Steehouwer, M., Dunwoodie, S. L., Schmiedeke, E., Märzheuser, S., Schwarzer, N., Brooks, A. S., de Klein, A., Sloots, C. E. J., Tibboel, D., Brisighelli, G., Morandi, A., Bedeschi, M. F., Bates, M. D., Levitt, M. A., Peña, A., de Blaauw, I., Roeleveld, N., Brunner, H. G., van Rooij, I. A. L. M., & Hoischen, A. (2020). A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Frontiers in pediatrics, 8310. https://doi.org/10.3389/fped.2020.00310
van de Putte, Romy, et al. "A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies." Frontiers in pediatrics vol. 8 (2020): 310. doi: https://doi.org/10.3389/fped.2020.00310
van de Putte R, Dworschak GC, Brosens E, Reutter HM, Marcelis CLM, Acuna-Hidalgo R, Kurtas NE, Steehouwer M, Dunwoodie SL, Schmiedeke E, Märzheuser S, Schwarzer N, Brooks AS, de Klein A, Sloots CEJ, Tibboel D, Brisighelli G, Morandi A, Bedeschi MF, Bates MD, Levitt MA, Peña A, de Blaauw I, Roeleveld N, Brunner HG, van Rooij IALM, Hoischen A. A Genetics-First Approach Revealed Monogenic Disorders in Patients With ARM and VACTERL Anomalies. Front Pediatr. 2020 Jun 23;8:310. doi: 10.3389/fped.2020.00310. eCollection 2020. PMID: 32656166; PMCID: PMC7324789.
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