Ribeiro, Lucilene Arilho; Bertolacini, Claudia Danielli Pereira; Quiezi, Rodrigo Gonçalves; Richieri-Costa, Antonio 
Source: Clinical Dysmorphology. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, PROTEÍNAS DO TECIDO NERVOSO, FENÓTIPOS, IMAGEM POR RESSONÂNCIA MAGNÉTICA
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RIBEIRO, Lucilene Arilho et al. A novel heterozygous missense mutation G316D of SIX3 gene in a brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis. Clinical Dysmorphology, v. 20, n. 3, p. 160-162, 2011Tradução . . Disponível em: https://doi.org/10.1097/MCD.0b013e32834116ae. Acesso em: 17 nov. 2024.APA
Ribeiro, L. A., Bertolacini, C. D. P., Quiezi, R. G., & Richieri-Costa, A. (2011). A novel heterozygous missense mutation G316D of SIX3 gene in a brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis. Clinical Dysmorphology, 20( 3), 160-162. doi:10.1097/MCD.0b013e32834116aeNLM
Ribeiro LA, Bertolacini CDP, Quiezi RG, Richieri-Costa A. A novel heterozygous missense mutation G316D of SIX3 gene in a brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis [Internet]. Clinical Dysmorphology. 2011 ; 20( 3): 160-162.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/MCD.0b013e32834116aeVancouver
Ribeiro LA, Bertolacini CDP, Quiezi RG, Richieri-Costa A. A novel heterozygous missense mutation G316D of SIX3 gene in a brazilian patient with holoprosencephaly-like phenotype and Langerhans cell histiocytosis [Internet]. Clinical Dysmorphology. 2011 ; 20( 3): 160-162.[citado 2024 nov. 17 ] Available from: https://doi.org/10.1097/MCD.0b013e32834116ae
