Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome
Author:
Funder
National Institutes of Health
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference16 articles.
1. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome;Ko;J Hum Genet,2008
2. Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome;Karow;Leukemia,2007
3. PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype;Bertola;Genet Test,2006
4. Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome;Hung;J Formos Med Assoc,2007
5. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity;Tartaglia;Am J Hum Genet,2002
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