PTPN11 Gene Analysis in 74 Brazilian Patients with Noonan Syndrome or Noonan-like Phenotype
Author:
Affiliation:
1. Clinical Genetics Unit, Instituto da Criança do Hospital das Clínicas, University of São Paulo, São Paulo, Brazil.
2. Laboratório de Genética e Cardiologia Molecular, Heart Institute (InCor), University of São Paulo, São Paulo, Brazil.
Publisher
Mary Ann Liebert Inc
Subject
Genetics(clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/gte.2006.10.186
Reference27 articles.
1. Occurrence of myeloproliferative disorder in patients with Noonan syndrome
2. Different mutations in theNF1 gene are associated with Neurofibromatosis-Noonan syndrome (NFNS)
3. Clinical variability in a Noonan syndrome family with a newPTPN11 gene mutation
4. Neurofibromatosis-Noonan syndrome: Molecular evidence of the concurrence of both disorders in a patient
5. NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
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