Source: The American Journal of Human Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DIAGNÓSTICO CLÍNICO
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MILLER, David T. et al. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, v. 86 n. 5, p. 749-764, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2010.04.006. Acesso em: 31 out. 2024.APA
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., et al. (2010). Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, 86 n. 5, 749-764. doi:10.1016/j.ajhg.2010.04.006NLM
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006Vancouver
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2024 out. 31 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006