References
- Rauen KA. The RASopathies. Annu Rev Genomics Hum Genet 2013; 14: 355-69.10.1146/annurev-genom-091212-153523
- Kaplan MS, Optiz JM, Cosset FR. Noonan’s syndrome: A case with elevated serum alkaline phosphatase levels and malignant schwannoma of the left forearm. Am J Dis Child 1968; 116(4): 359-66.569796810.1001/archpedi.1968.02100020363003
- Wyre HW Jr. Cutaneous manifestations of Noonan’s syndrome. Arch Dermatol 1978; 114(6): 929-30.10.1001/archderm.1978.01640180063015666330
- Allanson JE. Noonan syndrome. J Med Genet 1987;24(1):9-13.10.1136/jmg.24.1.93543368
- Sharland M, Burch M, McKenna WM, Patton MA. A clinical study of Noonan syndrome. Arch Dis Child 1992; 67(2):178-183.154337510.1136/adc.67.2.178
- Smpokou P, Tworog-Dube E, Kucherlapati RS, Roberts AE. Medical complications, clinical findings and educational outcomes in adults with Noonan syndrome. Am J Med Genet A 2012; 158A(12): 3106-3111.2316575110.1002/ajmg.a.35639
- Joyce S, Gordon K, Brice G, Ostergaard P, Nagaraja R, Short J, Moore S, Mortimer P, Mansour S. The lymphatic phenotype in Noonan and Cardiofaciocutaneous syndrome. Eur J Hum Genet. 2016; 24(5): 690-6.2624298810.1038/ejhg.2015.175
- Tartaglia M, Niemeyer CM, Fragale A, Song X, Buechner J, Jung A, Hählen K, Hasle H, Licht JD, Gelb BD. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia. Nat Genet 2003; 34(2): 148-50.1271743610.1038/ng1156
- Stark M, Assum G, Krone W. A small deletion and an adjacent base exchange in a potential stem-loop region of the neurofibromatosis 1 gene. Hum Genet 1991; 87(6): 685-87.
- Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, Brunner HG, Bertola DR, Crosby A, Ion A, Kucherlapati RS, Jeffery S, Patton MA, Gelb BD. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet 2002; 70(6): 1555-63.1199226110.1086/340847
- Rauen KA. Cardiofaciocutaneous syndrome. In: RA Pagon, MP Adam, HH Ardinger, SE Wallace, A Amemiya, LJH Bean, et al., editors. GeneReviews. 2016. Seattle (WA).
- Brouillard P, Boon L, Vikkula M. Genetics of lymphatic anomalies. J Clin Invest 2014; 124(3): 898-904.2459027410.1172/JCI71614
- Allanson JE, Roberts AE. Noonan Syndrome. In: RA Pagon, MP Adam, HH Ardinger, SE Wallace, A Amemiya, LJH Bean, et al., editors. GeneReviews. 2001. Seattle (WA).