Results 1 -
10
of
31
for
Noonan syndrome 4
- ... Testing Registry: Noonan syndrome 3 Genetic Testing Registry: Noonan syndrome 4 Genetic Testing Registry: Noonan syndrome 5 Genetic Testing ... NOONAN SYNDROME 1; NS1 NOONAN SYNDROME 2; NS2 NOONAN SYNDROME 4; NS4 NOONAN SYNDROME 3; NS3 NOONAN SYNDROME 5; ...
- ... Germline gain-of-function mutations in SOS1 cause Noonan syndrome. Nat Genet. 2007 Jan;39(1):70-4. doi: 10.1038/ng1926. Epub 2006 Dec 3. ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, ... Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. ...
- ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. ...
- ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. ...
- ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. ...
- ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. ...
- ... Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct;126(4):746-59. doi: 10.1542/peds.2009-3207. ...
- ... to cause this condition. The remaining individuals with Noonan syndrome with multiple lentigines do not have an identified mutation in any of these four genes. In these individuals, the cause of the ...
- ... A, Margalit E. Ocular manifestations of Donnai-Barrow syndrome. J Child Neurol. 2007 Apr;22(4):462-4. doi: 10.1177/0883073807301933. Citation on PubMed Pober BR, Longoni M, Noonan KM. A review of Donnai-Barrow and facio- ...
- ... Erratum In: Nurse Pract. 2005 Jul;30(7):4. Citation on PubMed Huffmeier U, Zenker M, Hoyer J, Fahsold R, Rauch A. A variable combination of features of Noonan syndrome and neurofibromatosis type I are caused by mutations ...