Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment
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Title
Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment
Authors
Keywords
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Journal
EUROPEAN JOURNAL OF PEDIATRICS
Volume 171, Issue 1, Pages 51-58
Publisher
Springer Nature
Online
2011-05-17
DOI
10.1007/s00431-011-1487-5
References
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Related references
Note: Only part of the references are listed.- Heterozygous Germline Mutations in the CBL Tumor-Suppressor Gene Cause a Noonan Syndrome-like Phenotype
- (2010) Simone Martinelli et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutations
- (2010) Murat Derbent et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Noonan syndrome associated with both a new Jnk-activating familial SOS1 and a de novo RAF1 mutations
- (2010) Mauro Longoni et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- The face of Noonan syndrome: Does phenotype predict genotype
- (2010) Judith E. Allanson et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes
- (2010) Amanda Salem Brasil et al. Genetic Testing and Molecular Biomarkers
- Molecular and clinical analysis ofRAF1in Noonan syndrome and related disorders: dephosphorylation of serine 259 as the essential mechanism for mutant activation
- (2010) Tomoko Kobayashi et al. HUMAN MUTATION
- Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines
- (2010) A. A. Romano et al. PEDIATRICS
- Noonan Syndrome and Related Disorders: A Review of Clinical Features and Mutations in Genes of the RAS/MAPK Pathway
- (2009) Alexander A.L. Jorge et al. Hormone Research in Paediatrics
- Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
- (2009) Viviana Cordeddu et al. NATURE GENETICS
- A restricted spectrum of NRAS mutations causes Noonan syndrome
- (2009) Ion C Cirstea et al. NATURE GENETICS
- Coinheritance of Noonan syndrome and Becker muscular dystrophy
- (2009) Argirios Dinopoulos et al. NEUROMUSCULAR DISORDERS
- Analysis of thePTPN11gene in idiopathic short stature children and Noonan syndrome patients
- (2008) Lize V. Ferreira et al. CLINICAL ENDOCRINOLOGY
- Clinical and molecular characterization of 40 patients with Noonan syndrome
- (2008) Giovanni Battista Ferrero et al. European Journal of Medical Genetics
- Protein tyrosine phosphatases in the JAK/STAT pathway
- (2008) Dan Xu Frontiers in Bioscience-Landmark
- The molecular functions of Shp2 in the Ras/Mitogen-activated protein kinase (ERK1/2) pathway
- (2007) Marie Dance et al. CELLULAR SIGNALLING
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