Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia-Reference-Cited by-同舟云学术

Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia

Published:2016-01-13 Issue:8 Volume:24 Page:1124-1131
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Cavé Hélène,Caye Aurélie,Ghedira Nehla,Capri Yline,Pouvreau Nathalie,Fillot Natacha,Trimouille Aurélien,Vignal Cédric,Fenneteau Odile,Alembik Yves,Alessandri Jean-Luc,Blanchet Patricia,Boute Odile,Bouvagnet Patrice,David Albert,Dieux Coeslier Anne,Doray Bérénice,Dulac Olivier,Drouin-Garraud Valérie,Gérard Marion,Héron Delphine,Isidor Bertrand,Lacombe Didier,Lyonnet Stanislas,Perrin Laurence,Rio Marlène,Roume Joëlle,Sauvion Sylvie,Toutain Annick,Vincent-Delorme Catherine,Willems Marjorie,Baumann Clarisse,Verloes Alain

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2015273.pdf

Reference30 articles.

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3. Kratz CP, Franke L, Peters H et al: Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes. Br J Cancer 2015; 112: 1392–1397.

4. Bader-Meunier B, Tchernia G, Mielot F et al: Occurrence of myeloproliferative disorder in patients with Noonan syndrome. J Pediatr 1997; 130: 885–889.

5. Strullu M, Caye A, Lachenaud J et al: Juvenile myelomonocytic leukaemia and Noonan syndrome. J Med Genet 2014; 51: 689–697.

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