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Page 1
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):533. Hum Genet. 2005. PMID: 15988825 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Polora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):536. Hum Genet. 2005. PMID: 15991309 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):537. Hum Genet. 2005. PMID: 15991310 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Polora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):537. Hum Genet. 2005. PMID: 15991311 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):540. Hum Genet. 2005. PMID: 15991319 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):540. Hum Genet. 2005. PMID: 15991320 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):540. Hum Genet. 2005. PMID: 15991321 No abstract available.
Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.
Schumacher V, Vogel T, Leube B, Driemel C, Goecke T, Moeslein G, Royer-Pokora B. Schumacher V, et al. Among authors: moeslein g. Hum Genet. 2005 May;116(6):541. Hum Genet. 2005. PMID: 15991322 No abstract available.
LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome.
Volikos E, Robinson J, Aittomäki K, Mecklin JP, Järvinen H, Westerman AM, de Rooji FW, Vogel T, Moeslein G, Launonen V, Tomlinson IP, Silver AR, Aaltonen LA. Volikos E, et al. Among authors: moeslein g. J Med Genet. 2006 May;43(5):e18. doi: 10.1136/jmg.2005.039875. J Med Genet. 2006. PMID: 16648371 Free PMC article.
Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADalpha, and MO25alpha, in Peutz-Jeghers syndrome.
Alhopuro P, Katajisto P, Lehtonen R, Ylisaukko-Oja SK, Näätsaari L, Karhu A, Westerman AM, Wilson JH, de Rooij FW, Vogel T, Moeslein G, Tomlinson IP, Aaltonen LA, Mäkelä TP, Launonen V. Alhopuro P, et al. Among authors: moeslein g. Br J Cancer. 2005 Mar 28;92(6):1126-9. doi: 10.1038/sj.bjc.6602454. Br J Cancer. 2005. PMID: 15756273 Free PMC article.
61 results