Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference

Meral Gunay-Aygun, Ellis D. Avner, Robert L. Bacallao, Peter L. Choyke, Joseph T. Flynn, Gregory G. Germino, Lisa Guay-Woodford, Peter Harris, Theo Heller, Julie Ingelfinger, Frederick Kaskel, Robert Kleta, Nicholas F. LaRusso, Parvathi Mohan, Gregory J. Pazour, Benjamin L. Shneider, Vicente E. Torres, Patricia Wilson, Colleen Zak, Jing ZhouWilliam A. Gahl

Research output: Contribution to journalArticle

55 Scopus citations
Original languageEnglish (US)
Pages (from-to)159-164
Number of pages6
JournalJournal of Pediatrics
Volume149
Issue number2
DOIs
StatePublished - Aug 2006

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Gunay-Aygun, M., Avner, E. D., Bacallao, R. L., Choyke, P. L., Flynn, J. T., Germino, G. G., Guay-Woodford, L., Harris, P., Heller, T., Ingelfinger, J., Kaskel, F., Kleta, R., LaRusso, N. F., Mohan, P., Pazour, G. J., Shneider, B. L., Torres, V. E., Wilson, P., Zak, C., ... Gahl, W. A. (2006). Autosomal recessive polycystic kidney disease and congenital hepatic fibrosis: Summary statement of a First National Institutes of Health/Office of Rare Diseases conference. Journal of Pediatrics, 149(2), 159-164. https://doi.org/10.1016/j.jpeds.2006.03.014