HuGE Literature Finder
Records
1
-
5
Clinical and molecular characterization of children with Noonan syndrome and other RASopathies in Argentina. Archivos argentinos de pediatria 2019 9 117 (5): 330-337. Chinton Josefina, Huckstadt Victoria, Moresco Angélica, Gravina L Pablo, Obregon M Gabrie |
Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients. Clinical genetics 2019 6 96 (4): 290-299. Li Xin, Yao Ruen, Tan Xin, Li Niu, Ding Yu, Li Juan, Chang Guoying, Chen Yao, Ma Lizhuang, Wang Jian, Fu Lijun, Wang Xium |
A genome-wide analysis of colorectal cancer in a child with Noonan syndrome. Pediatric blood & cancer 2018 7 65 (11): e27362. Prasad Rahul M, Mody Rajen J, Myers George, Mullins Melisa, Naji Zaher, Geiger James |
Runs of homozygosity associate with decreased risks of lung cancer in never-smoking East Asian females. Journal of Cancer 2018 9 (21): 3858-3866. Chen Yi-Xiao, Guo Yan, Dong Shan-Shan, Chen Xiao-Feng, Chen Jia-Bin, Zhang Yu-Jie, Yao Shi, Thynn Hlaing Nwe, Zhi Liqiang, Yang Tie-L |
Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. Human mutation 2009 Apr 30 (4): 695-702. Sarkozy Anna, Carta Claudio, Moretti Sonia, Zampino Giuseppe, Digilio Maria C, Pantaleoni Francesca, Scioletti Anna Paola, Esposito Giorgia, Cordeddu Viviana, Lepri Francesca, Petrangeli Valentina, Dentici Maria L, Mancini Grazia M S, Selicorni Angelo, Rossi Cesare, Mazzanti Laura, Marino Bruno, Ferrero Giovanni B, Silengo Margherita Cirillo, Memo Luigi, Stanzial Franco, Faravelli Francesca, Stuppia Liborio, Puxeddu Efisio, Gelb Bruce D, Dallapiccola Bruno, Tartaglia Mar |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 29, 2023
- Content source: