Clinical findings in patients with GLI2 mutations: phenotypic variability (2012)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1111/j.1399-0004.2010.01606.x
- Subjects: HOLOPROSENCEFALIA; ANORMALIDADES CRANIOFACIAIS; MUTAÇÃO
- Language: Inglês
- Imprenta:
- Publisher place: Copenhagen
- Date published: 2012
- Source:
- Título: Clinical Genetics
- ISSN: 0009-9163
- Volume/Número/Paginação/Ano: v. 81, n. 1, p. 70-75, Jan. 2012
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
BERTOLACINI, Claudia Danielli Pereira et al. Clinical findings in patients with GLI2 mutations: phenotypic variability. Clinical Genetics, v. 81, n. Ja 2012, p. 70-75, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2010.01606.x. Acesso em: 12 fev. 2026. -
APA
Bertolacini, C. D. P., Ribeiro-Bicudo, L. A., Petrin, A., Richieri-Costa, A., & Murray, J. C. (2012). Clinical findings in patients with GLI2 mutations: phenotypic variability. Clinical Genetics, 81( Ja 2012), 70-75. doi:10.1111/j.1399-0004.2010.01606.x -
NLM
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Clinical findings in patients with GLI2 mutations: phenotypic variability [Internet]. Clinical Genetics. 2012 ; 81( Ja 2012): 70-75.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1111/j.1399-0004.2010.01606.x -
Vancouver
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Clinical findings in patients with GLI2 mutations: phenotypic variability [Internet]. Clinical Genetics. 2012 ; 81( Ja 2012): 70-75.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1111/j.1399-0004.2010.01606.x - Noonan syndrome in diverse populations
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Informações sobre o DOI: 10.1111/j.1399-0004.2010.01606.x (Fonte: oaDOI API)
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