Freitas, Erika L; Gribble, Susan M; Simioni, Milena; Vieira, Társis P; Prigmore, Elena; Krepischi, Ana Cristina Victorino 
; Rosenberg, Carla ; Pearson, Peter L; Melo, Débora G; Lopes, Vera Lúcia Gil-da-Silva
Fonte: European Journal of Medical Genetics. Unidade: IB
Assuntos: MUTAÇÃO GENÉTICA, MALFORMAÇÕES, ANOMALIA CRANIOFACIAL, ACONSELHAMENTO GENÉTICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FREITAS, Erika L et al. A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state. European Journal of Medical Genetics, v. No 2012, n. 11, p. 660-665, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2012.06.015. Acesso em: 30 jun. 2024.APA
Freitas, E. L., Gribble, S. M., Simioni, M., Vieira, T. P., Prigmore, E., Krepischi, A. C. V., et al. (2012). A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state. European Journal of Medical Genetics, No 2012( 11), 660-665. doi:10.1016/j.ejmg.2012.06.015NLM
Freitas EL, Gribble SM, Simioni M, Vieira TP, Prigmore E, Krepischi ACV, Rosenberg C, Pearson PL, Melo DG, Lopes VLG-da-S. A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state [Internet]. European Journal of Medical Genetics. 2012 ; No 2012( 11): 660-665.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.ejmg.2012.06.015Vancouver
Freitas EL, Gribble SM, Simioni M, Vieira TP, Prigmore E, Krepischi ACV, Rosenberg C, Pearson PL, Melo DG, Lopes VLG-da-S. A familial case with interstitial 2q36 deletion: variable phenotypic expression in full and mosaic state [Internet]. European Journal of Medical Genetics. 2012 ; No 2012( 11): 660-665.[citado 2024 jun. 30 ] Available from: https://doi.org/10.1016/j.ejmg.2012.06.015
