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Article

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.

International journal of cardiology - 1 Jan 2015

Gulec Elif Yilmaz, Ocak Zeynep, Candan Sukru, Ataman Esra, Yarar Coskun

Abstract excerpt

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Topics

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Share to Phenotype
Share to Protein Tyrosine Phosphatase, Non-Receptor Type 11
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25804457
DOI: 10.1016/j.ijcard.2015.03.260

Genes

PTPN11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype.PMID 25804457Read ↗

Mutation Spectrum and Phenotypic Features in Noonan Syndrome with PTPN11 Mutations: Definition of Two Novel Mutations.Semantic proximity Read ↗

Spectrum of Mutations in PTPN11 in Russian Cohort.Semantic proximity Read ↗

Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.Semantic proximity Read ↗

Probable Noonan syndrome in a boy without PTPN11 mutation, manifesting unusual complications.Semantic proximity Read ↗

Variants of the PTPN11 Gene in Mexican Patients with Noonan Syndrome.Semantic proximity Read ↗

[Noonan's syndrome caused by a mutation in the PTPN11 gene].Semantic proximity Read ↗

A novel PTPN11 missense mutation in a patient with LEOPARD syndrome.Semantic proximity Read ↗

Novel mutations and their genotype-phenotype correlations in patients with Noonan syndrome, using next-generation sequencing.Semantic proximity Read ↗

Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment.Semantic proximity Read ↗

Clinical Variability in a Family with Noonan Syndrome with a Homozygous PTPN11 Gene Variant in Two IndividualsSemantic proximity Read ↗

Mutational analysis of PTPN11 gene in Taiwanese children with Noonan syndrome.Semantic proximity Read ↗

Noonan syndrome.Semantic proximity Read ↗

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