Source: American Journal of Medical Genetics. Unidade: FMRP
Assunto: MALFORMAÇÕES (GENÉTICA)
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ABNT
SCHANZE, Denny et al. Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders. American Journal of Medical Genetics, v. 161A, n. 12, p. 3012\20133017, 2013Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.36119. Acesso em: 15 out. 2024.APA
Schanze, D., Harakalova, M., Stevens, C. A., Brancati, F., Dallapiccola, B., Farndon, P., et al. (2013). Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders. American Journal of Medical Genetics, 161A( 12), 3012\20133017. doi:10.1002/ajmg.a.36119NLM
Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE de F, McGinn DMMD, Zackai EH, Wright M, Lieshout S van, Vogel MJ, Haelst MM van, Zenker M. Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders [Internet]. American Journal of Medical Genetics. 2013 ; 161A( 12): 3012\20133017.[citado 2024 out. 15 ] Available from: https://doi.org/10.1002/ajmg.a.36119Vancouver
Schanze D, Harakalova M, Stevens CA, Brancati F, Dallapiccola B, Farndon P, Ferraz VE de F, McGinn DMMD, Zackai EH, Wright M, Lieshout S van, Vogel MJ, Haelst MM van, Zenker M. Ablepharon macrostomia syndrome: a distinct genetic entity clinically related to the group of FRAS–FREM complex disorders [Internet]. American Journal of Medical Genetics. 2013 ; 161A( 12): 3012\20133017.[citado 2024 out. 15 ] Available from: https://doi.org/10.1002/ajmg.a.36119
