Molecular and clinical delineation of the 17q22 microdeletion phenotype (2013)
Laurell, Tobias; Lundin, Johanna; Anderlid, Britt-Marie; Gorski, Jerome L; Grigelioniene, Giedre; Knight, Samantha J. L; Krepischi, Ana Cristina Victorino 
; Nordenskjöld, Agneta; Price, Susan M; Rosenberg, Carla ; Turnpenny, Peter D; Vianna-Morgante, Angela M ; Nordgren, Ann
Source: European Journal of Human Genetics. Unidade: IB
Subjects: FENÓTIPOS, ANOMALIA FACIAL, RETARDO MENTAL, GENÉTICA MÉDICA
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LAURELL, Tobias et al. Molecular and clinical delineation of the 17q22 microdeletion phenotype. European Journal of Human Genetics, v. 21, n. 10, p. 1085-1092, 2013Tradução . . Disponível em: https://doi.org/10.1038/ejhg.2012.306. Acesso em: 13 nov. 2024.APA
Laurell, T., Lundin, J., Anderlid, B. -M., Gorski, J. L., Grigelioniene, G., Knight, S. J. L., et al. (2013). Molecular and clinical delineation of the 17q22 microdeletion phenotype. European Journal of Human Genetics, 21( 10), 1085-1092. doi:10.1038/ejhg.2012.306NLM
Laurell T, Lundin J, Anderlid B-M, Gorski JL, Grigelioniene G, Knight SJL, Krepischi ACV, Nordenskjöld A, Price SM, Rosenberg C, Turnpenny PD, Vianna-Morgante AM, Nordgren A. Molecular and clinical delineation of the 17q22 microdeletion phenotype [Internet]. European Journal of Human Genetics. 2013 ; 21( 10): 1085-1092.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/ejhg.2012.306Vancouver
Laurell T, Lundin J, Anderlid B-M, Gorski JL, Grigelioniene G, Knight SJL, Krepischi ACV, Nordenskjöld A, Price SM, Rosenberg C, Turnpenny PD, Vianna-Morgante AM, Nordgren A. Molecular and clinical delineation of the 17q22 microdeletion phenotype [Internet]. European Journal of Human Genetics. 2013 ; 21( 10): 1085-1092.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/ejhg.2012.306
