Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Noonan syndrome: The changing phenotype;Allanson;Am J Med Genet,1985
2. Noonan syndrome;Allanson;J Med Genet,1987
3. Noonan syndrome;Allanson;Am J Med Genet Part C,2007
4. Occurrence of myeloproliferative disorder in patients with Noonan syndrome;Bader-Meunier;J Pediatr,1997
5. Hematological findings in Noonan syndrome;Bertola;Rev Hosp Clin Fac Med Sao Paulo,2003
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