Gamba, Bruno Faulin; Richieri-Costa, Antonio 
; Costa, Silvia; Rosenberg, Carla ; Ribeiro-Bicudo, Lucilene Arilho
Source: Molecular Genetics and Genomics. Unidades: HRAC, IB
Subjects: DOENÇAS GENÉTICAS, CROMOSSOMOS HUMANOS (ANOMALIAS), MALFORMAÇÕES
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GAMBA, Bruno Faulin et al. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, n. Ju 2015, p. on-line, 2015Tradução . . Disponível em: https://doi.org/10.1007/s00438-015-1072-0. Acesso em: 14 nov. 2024.APA
Gamba, B. F., Richieri-Costa, A., Costa, S., Rosenberg, C., & Ribeiro-Bicudo, L. A. (2015). Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, ( Ju 2015), on-line. doi:10.1007/s00438-015-1072-0NLM
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s00438-015-1072-0Vancouver
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 nov. 14 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
