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Mutational analysis of theMRP2gene and long-term follow-up of Dubin-Johnson syndrome in Japan

โœ Scribed by Ikuo Machida; Shinya Wakusawa; Fujiko Sanae; Hisao Hayashi; Atsushi Kusakabe; Hiroshi Ninomiya; Motoyoshi Yano; Kentaro Yoshioka


Publisher
Springer Japan
Year
2005
Tongue
English
Weight
186 KB
Volume
40
Category
Article
ISSN
0944-1174

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Zimmermann-Laband syndrome in an adult.
โœ Robertson, Stephen P.; Lipp, Harry; Bankier, Agnes ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 37 KB ๐Ÿ‘ 2 views

Zimmermann-Laband syndrome (ZLS) is characterised by findings of coarse facial appearance, hepatosplenomegaly, and hirsutism often first observed in infancy, followed by the evolution during childhood of gingival fibromatosis, small joint hyperextensibility, and hypoplasia of the finger-and toenails