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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Rare Diseases

Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Short Bowel Syndrome[original query]
Introducing genetic testing for adult-type hypolactasia.
Digestion 2005 71 (4): 245-50.
Büning Carsten, Genschel Janine, Jurga Juliane, Fiedler Thomas, Voderholzer Winfried, Fiedler Eva-Maria, Worm Margitta, Weltrich Renita, Lochs Herbert, Schmidt Hartmut, Ockenga Joha
NOD2 mutations are associated with the development of intestinal failure in the absence of Crohn's disease.
Clinical nutrition (Edinburgh, Scotland) 2013 Dec 32 (6): 1029-35.
Schäffler Holger, Schneider Nina, Hsieh Chih-Jen, Reiner Johannes, Nadalin Silvio, Witte Maria, Königsrainer Alfred, Blumenstock Gunnar, Lamprecht Geo
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