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Alagille Syndrome: Difference between revisions
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==Links== | ==Links== | ||
*[http://www.scielo.org.ar/pdf/aap/v113n4/en_v113n4a21.pdf Liver mass containing normal bile ducts in an Alagille patient: A case report] | *[http://www.scielo.org.ar/pdf/aap/v113n4/en_v113n4a21.pdf Liver mass containing normal bile ducts in an Alagille patient: A case report] | ||
*[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489410/pdf/pone.0130355.pdf | *: Li L, Dong J, Wang X, Guo H, Wang H,Zhao J, et al. (2015) JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome. PLoS ONE 10(6): e0130355. doi:10.1371/journal.pone.0130355 [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4489410/pdf/pone.0130355.pdf open access full article ] | ||
==Notes== | ==Notes== | ||
<references/> | <references/> | ||
Revision as of 18:17, 23 July 2015
Alagylle syndrom is a multisystemic disease autosomal dominant, with variable expression [1]
Disease classification WHO
Q44.7 Allagille syndrome
Links
- Liver mass containing normal bile ducts in an Alagille patient: A case report
- Li L, Dong J, Wang X, Guo H, Wang H,Zhao J, et al. (2015) JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome. PLoS ONE 10(6): e0130355. doi:10.1371/journal.pone.0130355 open access full article