2 results  1 of 1 

1 Hereditary Spherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II
Shigeo Iijima, Takehiko Ohzeki, Yoshihiro Maruo
Yonsei Med J.2011;52(2):369-372.   Published online 2011 January 29     DOI: http://dx.doi.org/10.3349/ymj.2011.52.2.369
      
2 A Case of Crigler-Najjar Syndrome Type 2 Diagnosed Using Genetic Mutation Analysis
Sang Yee Kim, Soo Hyun Lee, Hong Koh, Seung Tae Lee, Chang Seok Ki, Jong Won Kim, Ki Sup Chung
Korean J Pediatr Gastroenterol Nutr.2008;11(2):219-222.   Published online 2008 September 30     DOI: http://dx.doi.org/10.5223/kjpgn.2008.11.2.219
      

 1 of 1