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Filtros : "Smith, D P" Limpar

Filtros

Artigo de periodico
Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas (1995)
Eng, C; Crossey, P A; Mulligan, L M; Healey, C S; Houghton, C; Prowse, A; Chew, S L; Dahia, P L M; Oriordan, J L H; Toledo, S. P. A.; Smith, D P; Maher, E R
Source: Journal of Medical Genetics. Unidade: FM
Assunto: ENDOCRINOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENG, C et al. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, v. 32, n. 12, p. 934-7, 1995Tradução . . Disponível em: https://doi.org/10.1136/jmg.32.12.934. Acesso em: 07 out. 2024.
APA
Eng, C., Crossey, P. A., Mulligan, L. M., Healey, C. S., Houghton, C., Prowse, A., et al. (1995). Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas. Journal of Medical Genetics, 32( 12), 934-7. doi:10.1136/jmg.32.12.934
NLM
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 out. 07 ] Available from: https://doi.org/10.1136/jmg.32.12.934
Vancouver
Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PLM, Oriordan JLH, Toledo SPA, Smith DP, Maher ER. Mutations in the ret proto-oncogene and the von hippel-lindau disease tumour supressor gene in sporadic and syndromic phaeochromocytomas [Internet]. Journal of Medical Genetics. 1995 ;32( 12): 934-7.[citado 2024 out. 07 ] Available from: https://doi.org/10.1136/jmg.32.12.934
Artigo de periodico
Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours (1994)
Eng, C; Smith, D P; Mulligan, L M; Nagai, Maria Aparecida; Healey, C S; Ponder, M A; Gardner, E; Schelimann, G F W; Jackson, C E; Tunnacliffe, A; Ponder, B A J
Source: Human Molecular Genetics. Unidade: FM
Assunto: ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ENG, C et al. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours. Human Molecular Genetics, v. 3 , n. 2 , p. 237-41, 1994Tradução . . Disponível em: https://doi.org/10.1093/hmg/3.2.237. Acesso em: 07 out. 2024.
APA
Eng, C., Smith, D. P., Mulligan, L. M., Nagai, M. A., Healey, C. S., Ponder, M. A., et al. (1994). Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours. Human Molecular Genetics, 3 ( 2 ), 237-41. doi:10.1093/hmg/3.2.237
NLM
Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Schelimann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours [Internet]. Human Molecular Genetics. 1994 ;3 ( 2 ): 237-41.[citado 2024 out. 07 ] Available from: https://doi.org/10.1093/hmg/3.2.237
Vancouver
Eng C, Smith DP, Mulligan LM, Nagai MA, Healey CS, Ponder MA, Gardner E, Schelimann GFW, Jackson CE, Tunnacliffe A, Ponder BAJ. Point mutation within the tyrosine kinase domain of the ret proto-oncogene in multiple endocrine neoplasia type 2b and related sporadic tumours [Internet]. Human Molecular Genetics. 1994 ;3 ( 2 ): 237-41.[citado 2024 out. 07 ] Available from: https://doi.org/10.1093/hmg/3.2.237

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