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2007 | 1 |
2010 | 2 |
2024 | 0 |
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SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome.
J Med Genet. 2007 Oct;44(10):651-6. doi: 10.1136/jmg.2007.051276. Epub 2007 Jun 23.
J Med Genet. 2007.
PMID: 17586837
Free PMC article.
Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations.
Longoni M, Moncini S, Cisternino M, Morella IM, Ferraiuolo S, Russo S, Mannarino S, Brazzelli V, Coi P, Zippel R, Venturin M, Riva P.
Longoni M, et al.
Am J Med Genet A. 2010 Sep;152A(9):2176-84. doi: 10.1002/ajmg.a.33564.
Am J Med Genet A. 2010.
PMID: 20683980
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Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.
Denayer E, Devriendt K, de Ravel T, Van Buggenhout G, Smeets E, Francois I, Sznajer Y, Craen M, Leventopoulos G, Mutesa L, Vandecasseye W, Massa G, Kayserili H, Sciot R, Fryns JP, Legius E.
Denayer E, et al.
Genes Chromosomes Cancer. 2010 Mar;49(3):242-52. doi: 10.1002/gcc.20735.
Genes Chromosomes Cancer. 2010.
PMID: 19953625
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