Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 2 (of 2 Records) |
Query Trace: Mulibrey Nanism[original query] |
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Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management. The Journal of pediatrics 2017 08 187 206-212.e1. Meyer Robert, Soellner Lukas, Begemann Matthias, Dicks Severin, Fekete György, Rahner Nils, Zerres Klaus, Elbracht Miriam, Eggermann Thom |
Liver pathology and biochemistry in patients with mutations in TRIM37 gene (Mulibrey nanism). Liver international : official journal of the International Association for the Study of the Liver 2022 2 42 (6): 1369-1378. Sivunen Johanna, Karlberg Susann, Kivisaari Reetta, Lohi Jouko, Karlberg Niklas, Jokinen Eero, Sarkola Taisto, Jahnukainen Timo, Lipsanen-Nyman Marita, Jalanko Han |
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