The Journal of Pediatrics
Volume 149, Issue 2 , Pages 159-164 , August 2006

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

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 Supported in part by the Intramural Research Program of the NIH, specifically, that of the National Human Genome Research Institute, and by the Office of Rare Diseases, Office of the Director, NIH, and ARPKD/CHF Alliance.

PII: S0022-3476(06)00186-7

doi: 10.1016/j.jpeds.2006.03.014

The Journal of Pediatrics
Volume 149, Issue 2 , Pages 159-164 , August 2006

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