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Filtros : "Schwartz, Charles E." Limpar

Filtros

Collaboration
Normalized affiliation
Non normalized affiliation
- a.c. camargo hospital, são paulo, brazil (1)
- cambridge institute of medical research, cambridge, uk (1)
- cambridge institute of medical research, cambridge, uk; institute of cancer research, surrey, uk (1)
- centre hospitalier régional universitaire de tours, service de genetique, inserm u930, tours, france (1)
- centre hospitalier universitaire de tours, service de génétique, f-37044 tours, france (1)

Artigo de periodico
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation (2010)
Lugtenberg, Dorien; Zangrande-Vieira, Luiz; Kirchhoff, Maria; Whibley, Annabel C.; Oudakker, Astrid R.; Kjaergaard, Susanne; Vianna-Morgante, Angela M ; Kleefstra, Tjitske; Ruiter, Mariken; Jehee, Fernanda S.; Ullmann, Reinhard; Schwartz, Charles E.; Stratton, Michael; Raymond, F. Lucy; Veltman, Joris A.; Vrijenhoek, Terry; Pfundt, Rolph; Schuurs-Hoeijmakers, Janneke H. M.; Hehir-Kwa, Jayne y.; Froyen, Guy; Chelly, Jamel; Ropers, Hans Hilger; Moraine, Claude; Gècz, Jozef; Knijnenburg, Jeroen; Kant, Sarina G.; Hamel, Ben C. J.; Resenberg, Carla; Bokhoven, Hans van; Brouwer, Arjan P. M. de
Source: American Journal of Medical Genetics Part A. Unidade: IB
Subjects: GENÉTICA, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LUGTENBERG, Dorien et al. Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation. American Journal of Medical Genetics Part A, v. 152A n. 3, p. 638-645, 2010Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.33292. Acesso em: 17 nov. 2024.
APA
Lugtenberg, D., Zangrande-Vieira, L., Kirchhoff, M., Whibley, A. C., Oudakker, A. R., Kjaergaard, S., et al. (2010). Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation. American Journal of Medical Genetics Part A, 152A n. 3, 638-645. doi:10.1002/ajmg.a.33292
NLM
Lugtenberg D, Zangrande-Vieira L, Kirchhoff M, Whibley AC, Oudakker AR, Kjaergaard S, Vianna-Morgante AM, Kleefstra T, Ruiter M, Jehee FS, Ullmann R, Schwartz CE, Stratton M, Raymond FL, Veltman JA, Vrijenhoek T, Pfundt R, Schuurs-Hoeijmakers JHM, Hehir-Kwa J y., Froyen G, Chelly J, Ropers HH, Moraine C, Gècz J, Knijnenburg J, Kant SG, Hamel BCJ, Resenberg C, Bokhoven H van, Brouwer APM de. Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation [Internet]. American Journal of Medical Genetics Part A. 2010 ; 152A n. 3 638-645.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.33292
Vancouver
Lugtenberg D, Zangrande-Vieira L, Kirchhoff M, Whibley AC, Oudakker AR, Kjaergaard S, Vianna-Morgante AM, Kleefstra T, Ruiter M, Jehee FS, Ullmann R, Schwartz CE, Stratton M, Raymond FL, Veltman JA, Vrijenhoek T, Pfundt R, Schuurs-Hoeijmakers JHM, Hehir-Kwa J y., Froyen G, Chelly J, Ropers HH, Moraine C, Gècz J, Knijnenburg J, Kant SG, Hamel BCJ, Resenberg C, Bokhoven H van, Brouwer APM de. Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation [Internet]. American Journal of Medical Genetics Part A. 2010 ; 152A n. 3 638-645.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1002/ajmg.a.33292
Artigo de periodico
Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair (2008)
Bauters, Marijke; Van Esch, Hilde; Friez, Michael J.; Boespflug-Tanguy, Odile; Zenker, Martin; Vianna-Morgante, Angela M ; Rosenberg, Carla ; Ignatius, Jaakko; Raynaud, Martine; Hollanders, Karen; Govaerts, Karen; Vandenreijt, Kris; Niel, Florence; Blanc, Pierre; Stevenson, Roger E.; Fryns, Jean-Pierre; Marynen, Peter; Schwartz, Charles E.; Froyen, Guy
Source: Genome Research. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, RETARDO MENTAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BAUTERS, Marijke et al. Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. Genome Research, v. 18, p. 847-858, 2008Tradução . . Disponível em: https://doi.org/10.1101/gr.075903.107. Acesso em: 17 nov. 2024.
APA
Bauters, M., Van Esch, H., Friez, M. J., Boespflug-Tanguy, O., Zenker, M., Vianna-Morgante, A. M., et al. (2008). Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. Genome Research, 18, 847-858. doi:10.1101/gr.075903.107
NLM
Bauters M, Van Esch H, Friez MJ, Boespflug-Tanguy O, Zenker M, Vianna-Morgante AM, Rosenberg C, Ignatius J, Raynaud M, Hollanders K, Govaerts K, Vandenreijt K, Niel F, Blanc P, Stevenson RE, Fryns J-P, Marynen P, Schwartz CE, Froyen G. Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair [Internet]. Genome Research. 2008 ; 18 847-858.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/gr.075903.107
Vancouver
Bauters M, Van Esch H, Friez MJ, Boespflug-Tanguy O, Zenker M, Vianna-Morgante AM, Rosenberg C, Ignatius J, Raynaud M, Hollanders K, Govaerts K, Vandenreijt K, Niel F, Blanc P, Stevenson RE, Fryns J-P, Marynen P, Schwartz CE, Froyen G. Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair [Internet]. Genome Research. 2008 ; 18 847-858.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1101/gr.075903.107

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