Source: Human Molecular Genetics. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, HOLOPROSENCEFALIA, FENÓTIPOS
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HONG, Sungkook et al. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome. Human Molecular Genetics, v. 25, n. 10, 2016Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddw064. Acesso em: 05 nov. 2024.APA
Hong, S., Hu, P., Marino, J., Hufnagel, S. B., Hopkin, R. J., Toromanovic, A., et al. (2016). Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome. Human Molecular Genetics, 25( 10). doi:10.1093/hmg/ddw064NLM
Hong S, Hu P, Marino J, Hufnagel SB, Hopkin RJ, Toromanovic A, Richieri-Costa A, Bicudo LAR, Kruszka P, Roessler E, Muenke M. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome [Internet]. Human Molecular Genetics. 2016 ; 25( 10):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/hmg/ddw064Vancouver
Hong S, Hu P, Marino J, Hufnagel SB, Hopkin RJ, Toromanovic A, Richieri-Costa A, Bicudo LAR, Kruszka P, Roessler E, Muenke M. Dominant-negative kinase domain mutations in FGFR1 can explain the clinical severity of Hartsfield syndrome [Internet]. Human Molecular Genetics. 2016 ; 25( 10):[citado 2024 nov. 05 ] Available from: https://doi.org/10.1093/hmg/ddw064
