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Nov. 30, 2016
References
  1. Conboy E, et al. Paraspinal neurofibromas and hypertrophic neuropathy in Noonan syndrome with multiple lentigines. Journal of Medical Genetics. 2016;53:123.
  2. Rojnueangnit K, et al. High incidence of Noonan syndrome features including short stature and pulmonic stenosis in patients carrying NF1 missense mutations affecting p.Arg1809: Genotype-phenotype correlation. Human Mutation. 2015;36:1052.
  3. Rogol AD. Causes of short stature. http://www.uptodate.com/home. Accessed June 26, 2016.
  4. Roberts AE, et al. Noonan syndrome. The Lancet. 2013;381:333.
  5. National Library of Medicine. Noonan syndrome. Genetics Home Reference. https://ghr.nlm.nih.gov/condition/noonan-syndrome. Accessed June 26, 2016.
  6. Romano AA, et al. Noonan syndrome: Clinical features, diagnosis, and management guidelines. Pediatrics. 2010;126:745.
  7. Learning about Noonan syndrome. National Human Genome Research Institute. https://www.genome.gov/25521674/learning-about-noonan-syndrome/. Accessed June 26, 2016.
  8. Noonan syndrome. Genetic and Rare Diseases Information Center. https://rarediseases.info.nih.gov/gard/10955/noonan-syndrome/resources/1. Accessed June 26, 2016.
  9. Noonan syndrome. National Organization for Rare Disorders. http://rarediseases.org/rare-diseases/noonan-syndrome/. Accessed June 26, 2016.
  10. Babovic-Vuksanovic D (expert opinion). Mayo Clinic, Rochester, Minn. June 29, 2016.