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Alagille Syndrome: Difference between revisions

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*Anad F et al. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1017275/pdf/jmedgene00050-0001.pdf Alagille..and deletion 20p]
*Anad F et al. [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1017275/pdf/jmedgene00050-0001.pdf Alagille..and deletion 20p]
*Meritxell Huch et al.Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver[http://www.cell.com/cell/pdf/S0092-8674(14)01566-9.pdf Cell 160:299-312, 2015]
*Meritxell Huch et al.Long-Term Culture of Genome-Stable Bipotent Stem Cells from Adult Human Liver[http://www.cell.com/cell/pdf/S0092-8674(14)01566-9.pdf Cell 160:299-312, 2015]
<ref>http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925268/pdf/ejhg2013140a.pdf</ref>
*[http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925268/pdf/ejhg2013140a.pdf]
*Stefano Zanotti and Ernesto Canalis. Notch Signaling In Skeletal Health and Disease [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501254/pdf/nihms690328.pdf Eur J Endocrinol. Author manuscript; available in PMC 2015 July 14.]
*Stefano Zanotti and Ernesto Canalis. Notch Signaling In Skeletal Health and Disease [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4501254/pdf/nihms690328.pdf Eur J Endocrinol. Author manuscript; available in PMC 2015 July 14.]



Revision as of 19:11, 23 July 2015

Alagylle syndrom is a multisystemic disease autosomal dominant, with variable expression [1][2]; with abnormalities of the liver, heart[3], eye, skeleton and a characteristic facial appearance[4]

Disease classification WHO
Q44.7 Allagille syndrome

Links

Notes

References

References: