Fonte: American Journal of Human Genetics. Nome do evento: Annual Meeting of the American Journal of Human Genetics. Unidades: FMRP, FORP
Assuntos: ANOMALIA CRANIOFACIAL, GENÉTICA MÉDICA
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ABNT
HANSING, S. E. et al. Lacunar skull and limb defect with 22q11 microdeletion: novel feature of velocario-facial syndrome ?. American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 21 out. 2025. , 2001APA
Hansing, S. E., Rosa, D. D., Machado, M. L., Passos, G. A. S., Ramos, E. S., & Garcia, P. S. (2001). Lacunar skull and limb defect with 22q11 microdeletion: novel feature of velocario-facial syndrome ? American Journal of Human Genetics. Chicago: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.NLM
Hansing SE, Rosa DD, Machado ML, Passos GAS, Ramos ES, Garcia PS. Lacunar skull and limb defect with 22q11 microdeletion: novel feature of velocario-facial syndrome ? American Journal of Human Genetics. 2001 ; 69( 4): 305.[citado 2025 out. 21 ]Vancouver
Hansing SE, Rosa DD, Machado ML, Passos GAS, Ramos ES, Garcia PS. Lacunar skull and limb defect with 22q11 microdeletion: novel feature of velocario-facial syndrome ? American Journal of Human Genetics. 2001 ; 69( 4): 305.[citado 2025 out. 21 ]
