Datasets
- 1 - 25 out of 51 results
Search results
-
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
-
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
-
Additional file 1 of Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma
Lo Faro, V. (Creator), ten Brink, J. (Creator), Snieder, H. (Creator), Jansonius, N. M. (Creator) & Bergen, A. A. (Creator), Figshare, 2021
DOI: 10.6084/m9.figshare.15110290, https://springernature.figshare.com/articles/dataset/Additional_file_1_of_Genome-wide_CNV_investigation_suggests_a_role_for_cadherin_Wnt_and_p53_pathways_in_primary_open-angle_glaucoma/15110290
Dataset
-
Additional file 1 of Genome-wide CNV investigation suggests a role for cadherin, Wnt, and p53 pathways in primary open-angle glaucoma
Lo Faro, V. (Creator), ten Brink, J. (Creator), Snieder, H. (Creator), Jansonius, N. M. (Creator) & Bergen, A. A. (Creator), Figshare, 2021
DOI: 10.6084/m9.figshare.15110290.v1, https://springernature.figshare.com/articles/dataset/Additional_file_1_of_Genome-wide_CNV_investigation_suggests_a_role_for_cadherin_Wnt_and_p53_pathways_in_primary_open-angle_glaucoma/15110290/1
Dataset
-
Additional file 1 of To continue or not to continue? Antipsychotic medication maintenance versus dose-reduction/discontinuation in first episode psychosis: HAMLETT, a pragmatic multicenter single-blind randomized controlled trial
Begemann, M. J. H. (Creator), Thompson, I. A. (Creator), Veling, W. (Creator), Gangadin, S. S. (Contributor), Geraets, C. N. W. (Creator), Van 'T Hag, E. (Contributor), Müller-Kuperus, S. J. (Creator), Oomen, P. P. (Creator), Voppel, A. E. (Creator), Van Der Gaag, M. (Contributor), Kikkert, M. J. (Creator), Van Os, J. (Contributor), Smit, H. F. E. (Contributor), Knegtering, R. H. (Creator), Wiersma, S. (Creator), Stouten, L. H. (Contributor), Gijsman, H. J. (Creator), Wunderink, L. (Creator), Staring, A. B. P. (Creator), Veerman, S. R. T. (Creator), Mahabir, A. G. S. (Creator), Kurkamp, J. (Creator), Pijnenborg, G. H. M. (Creator), Veen, N. D. (Creator), Marcelis, M. (Creator), Grootens, K. P. (Creator), Faber, G. (Creator), Van Beveren, N. J. (Contributor), Been, A. (Creator), Van Den Brink, T. (Contributor), Bak, M. (Creator), Van Amelsvoort, T. A. M. J. (Contributor), Ruissen, A. (Creator), Blanke, C. (Creator), Groen, K. (Creator), de Haan, L. (Contributor), Sommer, I. E. C. (Creator), Begemann, M. (Creator), Veling, W. (Creator), Kikkert, M. (Creator), Os, J. (Creator), Amelsvoort, T. (Creator), Groen, K. (Creator), Haan, L. (Creator) & Sommer, I. (Creator), Figshare, 2020
DOI: 10.6084/m9.figshare.11826258, https://springernature.figshare.com/articles/Additional_file_1_of_To_continue_or_not_to_continue_Antipsychotic_medication_maintenance_versus_dose-reduction_discontinuation_in_first_episode_psychosis_HAMLETT_a_pragmatic_multicenter_single-blind_randomized_controlled_trial/11826258
Dataset
-
Additional file 1 of To continue or not to continue? Antipsychotic medication maintenance versus dose-reduction/discontinuation in first episode psychosis: HAMLETT, a pragmatic multicenter single-blind randomized controlled trial
Begemann, M. J. H. (Creator), Thompson, I. A. (Creator), Veling, W. (Creator), Gangadin, S. S. (Contributor), Geraets, C. N. W. (Creator), Van 'T Hag, E. (Contributor), Müller-Kuperus, S. J. (Creator), Oomen, P. P. (Creator), Voppel, A. E. (Creator), Van Der Gaag, M. (Contributor), Kikkert, M. J. (Creator), Van Os, J. (Contributor), Smit, H. F. E. (Contributor), Knegtering, R. H. (Creator), Wiersma, S. (Creator), Stouten, L. H. (Contributor), Gijsman, H. J. (Creator), Wunderink, L. (Creator), Staring, A. B. P. (Creator), Veerman, S. R. T. (Creator), Mahabir, A. G. S. (Creator), Kurkamp, J. (Creator), Pijnenborg, G. H. M. (Creator), Veen, N. D. (Creator), Marcelis, M. (Creator), Grootens, K. P. (Creator), Faber, G. (Creator), Van Beveren, N. J. (Contributor), Been, A. (Creator), Van Den Brink, T. (Contributor), Bak, M. (Creator), Van Amelsvoort, T. A. M. J. (Contributor), Ruissen, A. (Creator), Blanke, C. (Creator), Groen, K. (Creator), de Haan, L. (Contributor), Sommer, I. E. C. (Creator), Begemann, M. (Creator), Veling, W. (Creator), Kikkert, M. (Creator), Os, J. (Creator), Amelsvoort, T. (Creator), Groen, K. (Creator), Haan, L. (Creator) & Sommer, I. (Creator), Figshare, 2020
DOI: 10.6084/m9.figshare.11826258.v1, https://springernature.figshare.com/articles/Additional_file_1_of_To_continue_or_not_to_continue_Antipsychotic_medication_maintenance_versus_dose-reduction_discontinuation_in_first_episode_psychosis_HAMLETT_a_pragmatic_multicenter_single-blind_randomized_controlled_trial/11826258/1
Dataset
-
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
-
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
-
Additional file 3: 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.7878887.v1, https://springernature.figshare.com/articles/Additional_file_3_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878887/1
Dataset
-
Additional file 3: 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.7878887, https://springernature.figshare.com/articles/Additional_file_3_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878887
Dataset
-
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
-
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, 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
Dataset
-
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
-
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.v1, https://springernature.figshare.com/articles/Additional_file_5_of_Genome-wide_methylation_profiling_of_Beckwith-Wiedemann_syndrome_patients_without_molecular_confirmation_after_routine_diagnostics/7878908/1
Dataset
-
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
-
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, 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
Dataset
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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