Datasets
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MOESM4 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252091, https://springernature.figshare.com/articles/MOESM4_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252091
Dataset
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MOESM3 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252082, https://springernature.figshare.com/articles/MOESM3_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252082
Dataset
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MOESM2 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252073, https://springernature.figshare.com/articles/MOESM2_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252073
Dataset
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MOESM3 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252082.v1, https://springernature.figshare.com/articles/MOESM3_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252082/1
Dataset
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MOESM4 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252091.v1, https://springernature.figshare.com/articles/MOESM4_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252091/1
Dataset
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MOESM5 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252100.v1, https://springernature.figshare.com/articles/MOESM5_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252100/1
Dataset
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Additional file 7: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878920.v1, https://springernature.figshare.com/articles/Additional_file_7_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878920/1
Dataset
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Additional file 2: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878881, https://springernature.figshare.com/articles/Additional_file_2_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878881
Dataset
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Additional file 8: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878923.v1, https://springernature.figshare.com/articles/Additional_file_8_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878923/1
Dataset
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Additional file 8: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878923, https://springernature.figshare.com/articles/Additional_file_8_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878923
Dataset
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Additional file 10: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878860.v1, https://springernature.figshare.com/articles/Additional_file_10_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878860/1
Dataset
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MOESM6 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252106, https://springernature.figshare.com/articles/MOESM6_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252106
Dataset
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MOESM1 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252070.v1, https://springernature.figshare.com/articles/MOESM1_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252070/1
Dataset
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MOESM1 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252070, https://springernature.figshare.com/articles/MOESM1_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252070
Dataset
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Data from: SYNGAP1 encephalopathy: a distinctive generalized developmental and epileptic encephalopathy
Vlaskamp, D. R. M. (Contributor), Shaw, B. J. (Contributor), Burgess, R. (Contributor), Mei, D. (Contributor), Montomoli, M. (Contributor), Xie, H. (Contributor), Myers, C. T. (Contributor), Bennett, M. F. (Contributor), Xiangwei, W. (Contributor), Williams, D. (Contributor), Maas, S. (Contributor), Brooks, A. S. (Contributor), Mancini, G. M. S. (Contributor), Van De Laar, I. M. B. H. (Contributor), Van Hagen, J. M. (Contributor), Ware, T. L. (Contributor), Webster, R. I. (Contributor), Malone, S. (Contributor), Berkovic, S. F. (Contributor), Kalnins, R. M. (Contributor), Sicca, F. (Contributor), Korenke, G. C. (Contributor), Van Ravenswaaij-Arts, C. M. A. (Contributor), Hildebrand, M. S. (Contributor), Mefford, H. C. (Contributor), Jiang, Y. (Contributor), Guerrini, R. (Contributor), Scheffer, I. E. (Contributor), Mancini, G. M. S. (Contributor), Webster, R. I. (Contributor) & Guerrini, R. (Contributor), ZENODO, 4 Sept 2019
DOI: 10.5061/dryad.ck70sj0, https://zenodo.org/record/5008573
Dataset
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Additional file 4: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878896.v1, https://springernature.figshare.com/articles/Additional_file_4_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878896/1
Dataset
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Additional file 9: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878926, https://springernature.figshare.com/articles/Additional_file_9_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878926
Dataset
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Additional file 9: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878926.v1, https://springernature.figshare.com/articles/Additional_file_9_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878926/1
Dataset
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Additional file 2: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878881.v1, https://springernature.figshare.com/articles/Additional_file_2_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878881/1
Dataset
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Additional file 10: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878860, https://springernature.figshare.com/articles/Additional_file_10_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878860
Dataset
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Additional file 5: of Genome-wide methylation profiling of Beckwith-Wiedemann syndrome patients without molecular confirmation after routine diagnostics
Krzyzewska, I. (Contributor), Alders, M. (Contributor), Maas, S. (Contributor), Bliek, J. (Contributor), Venema, A. (Contributor), Henneman, P. (Contributor), Rezwan, F. I. (Contributor), Lip, K. V. D. (Contributor), Mul, A. N. (Contributor), Mackay, D. J. G. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.7878908, https://springernature.figshare.com/articles/Additional_file_5_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878908
Dataset
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MOESM5 of A genome-wide DNA methylation signature for SETD1B-related syndrome
Krzyzewska, I. (Contributor), Maas, S. (Contributor), Henneman, P. (Contributor), Lip, K. V. D. (Contributor), Venema, A. (Contributor), Baranano, K. (Contributor), Chassevent, A. (Contributor), Aref-Eshghi, E. (Contributor), Fukuda, T. (Contributor), Ikeda, H. (Contributor), Jacquemont, M. (Contributor), Kim, H. (Contributor), Labalme, A. (Contributor), Lewis, S. M. E. (Contributor), Lesca, G. (Contributor), Madrigal, I. (Contributor), Mahida, S. (Contributor), Matsumoto, N. (Contributor), Rabionet, R. (Contributor), Rajcan-Separovic, E. (Contributor), Qiao, Y. (Contributor), Sadikovic, B. (Contributor), Saitsu, H. (Contributor), Sweetser, D. A. (Contributor), Alders, M. (Contributor) & Mannens, M. (Contributor), Figshare, 2019
DOI: 10.6084/m9.figshare.10252100, https://springernature.figshare.com/articles/MOESM5_of_A_genome-wide_DNA_methylation_signature_for_SETD1B-related_syndrome/10252100
Dataset
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Data from: SYNGAP1 encephalopathy: a distinctive generalized developmental and epileptic encephalopathy
Vlaskamp, D. R. M. (Creator), Shaw, B. J. (Creator), Burgess, R. (Creator), Mei, D. (Creator), Montomoli, M. (Creator), Xie, H. (Creator), Myers, C. T. (Creator), Bennett, M. F. (Creator), Xiangwei, W. (Contributor), Williams, D. (Creator), Maas, S. (Creator), Brooks, A. S. (Creator), Mancini, G. M. S. (Creator), Van De Laar, I. M. B. H. (Creator), Van Hagen, J. M. (Creator), Ware, T. L. (Creator), Webster, R. I. (Creator), Malone, S. (Creator), Berkovic, S. F. (Creator), Kalnins, R. M. (Creator), Sicca, F. (Creator), Korenke, G. C. (Creator), Van Ravenswaaij-Arts, C. M. A. (Creator), Hildebrand, M. S. (Creator), Mefford, H. C. (Creator), Jiang, Y. (Creator), Guerrini, R. (Creator), Scheffer, I. E. (Creator), Mancini, G. M. S. (Creator), Webster, R. I. (Creator) & Guerrini, R. (Creator), Dryad Digital Repository, 2019
DOI: 10.5061/dryad.ck70sj0.2, https://datadryad.org/resource/doi:10.5061/dryad.ck70sj0.2
Dataset
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Data from: SYNGAP1 encephalopathy: a distinctive generalized developmental and epileptic encephalopathy
Vlaskamp, D. R. M. (Creator), Shaw, B. J. (Creator), Burgess, R. (Creator), Mei, D. (Creator), Montomoli, M. (Creator), Xie, H. (Creator), Myers, C. T. (Creator), Bennett, M. F. (Creator), Xiangwei, W. (Contributor), Williams, D. (Creator), Maas, S. (Creator), Brooks, A. S. (Creator), Mancini, G. M. S. (Creator), Van De Laar, I. M. B. H. (Creator), Van Hagen, J. M. (Creator), Ware, T. L. (Creator), Webster, R. I. (Creator), Malone, S. (Creator), Berkovic, S. F. (Creator), Kalnins, R. M. (Creator), Sicca, F. (Creator), Korenke, G. C. (Creator), Van Ravenswaaij-Arts, C. M. A. (Creator), Hildebrand, M. S. (Creator), Mefford, H. C. (Creator), Jiang, Y. (Creator), Guerrini, R. (Creator), Scheffer, I. E. (Creator), Mancini, G. M. S. (Creator), Webster, R. I. (Creator) & Guerrini, R. (Creator), Dryad Digital Repository, 2018
DOI: 10.5061/dryad.ck70sj0.1, https://datadryad.org/resource/doi:10.5061/dryad.ck70sj0.1
Dataset
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Data from: SYNGAP1 encephalopathy: a distinctive generalized developmental and epileptic encephalopathy
Vlaskamp, D. R. M. (Creator), Shaw, B. J. (Creator), Burgess, R. (Creator), Mei, D. (Creator), Montomoli, M. (Creator), Xie, H. (Creator), Myers, C. T. (Creator), Bennett, M. F. (Creator), Xiangwei, W. (Contributor), Williams, D. (Creator), Maas, S. (Creator), Brooks, A. S. (Creator), Mancini, G. M. S. (Creator), Van De Laar, I. M. B. H. (Creator), Van Hagen, J. M. (Creator), Ware, T. L. (Creator), Webster, R. I. (Creator), Malone, S. (Creator), Berkovic, S. F. (Creator), Kalnins, R. M. (Creator), Sicca, F. (Creator), Korenke, G. C. (Creator), Van Ravenswaaij-Arts, C. M. A. (Creator), Hildebrand, M. S. (Creator), Mefford, H. C. (Creator), Jiang, Y. (Creator), Guerrini, R. (Creator), Scheffer, I. E. (Creator), Mancini, G. M. S. (Creator), Webster, R. I. (Creator) & Guerrini, R. (Creator), Dryad Digital Repository, 2019
DOI: 10.5061/dryad.ck70sj0, https://datadryad.org/resource/doi:10.5061/dryad.ck70sj0
Dataset