×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome.
28074573
2017
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
A PTPN11 allele encoding a catalytically impaired SHP2 protein in a patient with a Noonan syndrome phenotype.
24891296
2014
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome.
19020799
2008
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy.
15889278
2005
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient.
15948193
2005
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Clinical variability in a Noonan syndrome family with a new PTPN11 gene mutation.
15384080
2004
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes.
12960218
2003
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Noonan syndrome with leukaemoid reaction and overproduction of catecholamines: a case report.
12739139
2003
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia.
12717436
2003
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome.
12634870
2003
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning.
12529711
2003
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity.
11992261
2002
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
We surveyed 16 subjects with the clinical diagnosis of Noonan Syndrome (NS1 ) from 12 families and their relevant family members for mutations in PTPN11 /SHP2 using direct DNA sequencing.
12325025
2002
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
PTPN11 (protein-tyrosine phosphatase, nonreceptor-type 11) mutations in seven Japanese patients with Noonan syndrome.
12161469
2002
×
Entrez Id:
5781
Gene Symbol:
PTPN11
PTPN11
Noonan Syndrome 1
0.910
GeneticVariation
UNIPROT
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.
11704759
2001