PTPN11 Gene Analysis in 74 Brazilian Patients with Noonan Syndrome or Noonan-like Phenotype

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PTPN11 Gene Analysis in 74 Brazilian Patients with Noonan Syndrome or Noonan-like Phenotype is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/GTE.2006.10.186
P698PubMed publication ID17020470

P50authorJosé Eduardo KriegerQ37370842
Chong Ae KimQ40388281
Débora R BertolaQ51915156
P2093author name stringAlexandre C Pereira
Lílian Maria José Albano
Paulo S L De Oliveira
P433issue3
P921main subjectphenotypeQ104053
Noonan syndromeQ1543446
P304page(s)186-191
P577publication date2006-01-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titlePTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype
P478volume10

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cites work (P2860)
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Q34299836Clinical and Molecular Findings of Tunisian Patients with RASopathies
Q42749590Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?
Q47932289Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome
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Q90273272Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations
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Q33382063PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome
Q84136085Phenotypic spectrum of 80 Greek patients referred as Noonan syndrome and PTPN11 mutation analysis: the value of initial clinical assessment
Q54283112Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome.
Q54212177Retrospective study of prenatal ultrasound findings in newborns with a Noonan spectrum disorder.
Q34327160SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions
Q37159467The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders

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