Fonte: Journal of the American Society of Nephrology. Nome do evento: Abstracts issue journal of the american Society of Nephrology - JASN. Unidade: FM
Assuntos: RIM (PATOLOGIA), CISTOS (DIAGNÓSTICO;GENÉTICA), DOENÇAS BILIARES (DIAGNÓSTICO), GENÓTIPOS
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GALLAGHER, Rachel et al. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo. . Acesso em: 24 jul. 2024. , 2004APA
Gallagher, R., Esquivel, E., Tian, X., Samaroo, T., Jain, D., Onuchie, L., et al. (2004). Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. Baltimore: Faculdade de Medicina, Universidade de São Paulo.NLM
Gallagher R, Esquivel E, Tian X, Samaroo T, Jain D, Onuchie L, Woodford LG, Germino G, Somlo S. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. 2004 ; 15 56A res. SU-FC061.[citado 2024 jul. 24 ]Vancouver
Gallagher R, Esquivel E, Tian X, Samaroo T, Jain D, Onuchie L, Woodford LG, Germino G, Somlo S. Inactivation of PKHD1 results in a liver phenotype characteristic of autosomal recessive polycystic kidney disease (ARPKD). Journal of the American Society of Nephrology. 2004 ; 15 56A res. SU-FC061.[citado 2024 jul. 24 ]
