Joint involvement in Noonan syndrome. A retrospective paediatric descriptive study

Author:

Le Quellec Aurore,Edouard Thomas,Audebert-Bellanger Séverine,Pouzet Antoine,Bourdet Karine,Colson Cindy,Oriot Charlotte,Poignant Sylvaine,Saraux Alain,Devauchelle-Pensec Valérie

Publisher

Elsevier BV

Subject

Rheumatology

Reference25 articles.

1. The Ullrich-Noonan syndrome (Turner phenotype);Nora;Am J Dis Child,1974

2. Noonan syndrome-causing genes: molecular update and an assessment of the mutation rate;El Bouchikhi;Int J Pediatr Adolesc Med,2016

3. Noonan syndrome and clinically related disorders;Tartaglia;Best Pract Res Clin Endocrinol Metab,2011

4. Clinical and molecular studies in a large Dutch family with Noonan syndrome;van der Burgt;Am J Med Genet,1994

5. PTPN11 mutations are associated with mild growth hormone resistance in individuals with Noonan syndrome;Binder;J Clin Endocrinol Metab,2005

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