Clinical and molecular delineation of the 17q21.31 microdeletion syndrome (2008)
Koolen, D. A.; Sharp, A. J.; Hurst, J. A.; Firth, Helen V.; Knight, S. J. L.; Goldenberg, A.; Saugier-Veber, P.; Pfundt, R.; Vissers, L. E. L. M.; Destrée, A.; Grisart, B.; Rooms, L.; Van der Aa, N.; Field, M.; Hackett, A.; Bell, K.; Nowaczyk, M. J. M.; Mancini, G. M. S.; Poddighe, P. J.; Schwartz, C. E.; Rossi, E.; De Gregori, M.; Antonacci-Fulton, L. L.; McLellan II, M. D.; Garrett, J. M.; Wiechert, M A; Miner, T. L.; Crosby, S.; Ciccone, R; Willatt, Lionel; Rauch, A.; Zenker, Martin; Aradhya, S.; Manning, M. A.; Strom, T. M.; Wagenstaller, J.; Krepischi, Ana Cristina Victorino 
; Vianna-Morgante, Angela M ; Rosenberg, Carla ; Price, S. M.; Stewart, H; Shaw-Smith, Charles; Brunner, H. G.; Wilkie, A. O. M.; Veltman, J. A.; Zuffardi, O.; Eichler, E. E.; Vries, B. B. A.
Source: Journal of Medical Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, GENOMAS
ABNT
KOOLEN, D. A. et al. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. Journal of Medical Genetics, v. 45, n. 11, p. 710-720, 2008Tradução . . Disponível em: https://doi.org/10.1136/jmg.2008.058701. Acesso em: 13 nov. 2024.APA
Koolen, D. A., Sharp, A. J., Hurst, J. A., Firth, H. V., Knight, S. J. L., Goldenberg, A., et al. (2008). Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. Journal of Medical Genetics, 45( 11), 710-720. doi:10.1136/jmg.2008.058701NLM
Koolen DA, Sharp AJ, Hurst JA, Firth HV, Knight SJL, Goldenberg A, Saugier-Veber P, Pfundt R, Vissers LELM, Destrée A, Grisart B, Rooms L, Van der Aa N, Field M, Hackett A, Bell K, Nowaczyk MJM, Mancini GMS, Poddighe PJ, Schwartz CE, Rossi E, De Gregori M, Antonacci-Fulton LL, McLellan II MD, Garrett JM, Wiechert MA, Miner TL, Crosby S, Ciccone R, Willatt L, Rauch A, Zenker M, Aradhya S, Manning MA, Strom TM, Wagenstaller J, Krepischi ACV, Vianna-Morgante AM, Rosenberg C, Price SM, Stewart H, Shaw-Smith C, Brunner HG, Wilkie AOM, Veltman JA, Zuffardi O, Eichler EE, Vries BBA. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome [Internet]. Journal of Medical Genetics. 2008 ; 45( 11): 710-720.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1136/jmg.2008.058701Vancouver
Koolen DA, Sharp AJ, Hurst JA, Firth HV, Knight SJL, Goldenberg A, Saugier-Veber P, Pfundt R, Vissers LELM, Destrée A, Grisart B, Rooms L, Van der Aa N, Field M, Hackett A, Bell K, Nowaczyk MJM, Mancini GMS, Poddighe PJ, Schwartz CE, Rossi E, De Gregori M, Antonacci-Fulton LL, McLellan II MD, Garrett JM, Wiechert MA, Miner TL, Crosby S, Ciccone R, Willatt L, Rauch A, Zenker M, Aradhya S, Manning MA, Strom TM, Wagenstaller J, Krepischi ACV, Vianna-Morgante AM, Rosenberg C, Price SM, Stewart H, Shaw-Smith C, Brunner HG, Wilkie AOM, Veltman JA, Zuffardi O, Eichler EE, Vries BBA. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome [Internet]. Journal of Medical Genetics. 2008 ; 45( 11): 710-720.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1136/jmg.2008.058701
