Gamba, Bruno Faulin; Zechi-Ceide, Roseli Maria; Kokitsu-Nakata, Nancy Mizue; Vendramini-Pittoli, Siulan; Rosenberg, Carla 
; Santos, Ana Carolina Alves dos; Ribeiro-Bicudo, Lucilene Arilho; Richieri-Costa, Antonio
Source: Molecular Syndromology. Unidades: HRAC, IB
Subjects: ANORMALIDADES CONGÊNITAS, MICROCEFALIA, DEFICIÊNCIA MENTAL, DELEÇÃO DE GENES
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GAMBA, Bruno Faulin et al. Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability. Molecular Syndromology, v. 7, n. 6, p. 344-348, 2016Tradução . . Disponível em: https://doi.org/10.1159/000450971. Acesso em: 13 nov. 2024.APA
Gamba, B. F., Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., Vendramini-Pittoli, S., Rosenberg, C., Santos, A. C. A. dos, et al. (2016). Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability. Molecular Syndromology, 7( 6), 344-348. doi:10.1159/000450971NLM
Gamba BF, Zechi-Ceide RM, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Santos ACA dos, Ribeiro-Bicudo LA, Richieri-Costa A. Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability [Internet]. Molecular Syndromology. 2016 ; 7( 6): 344-348.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1159/000450971Vancouver
Gamba BF, Zechi-Ceide RM, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Santos ACA dos, Ribeiro-Bicudo LA, Richieri-Costa A. Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability [Internet]. Molecular Syndromology. 2016 ; 7( 6): 344-348.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1159/000450971
