PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes-Reference-Cited by-同舟云学术

PTPN11 and KRAS Gene Analysis in Patients with Noonan and Noonan-Like Syndromes

Published:2010-06 Issue:3 Volume:14 Page:425-432
ISSN:1945-0265
Container-title:Genetic Testing and Molecular Biomarkers
language:en
Short-container-title:Genetic Testing and Molecular Biomarkers

Author:

Brasil Amanda Salem¹,Pereira Alexandre C.²,Wanderley Luciana Turolla¹,Kim Chong Ae¹,Malaquias Alexsandra C.³,Jorge Alexander A.L.³,Krieger José Eduardo²,Bertola Débora Romeo¹

Affiliation:

1. Unidade de Genética, Instituto da Criança, São Paulo, Brazil.

2. Laboratório de Genética e Cardiologia Molecular, InCor, São Paulo, Brazil.

3. Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormôminos e Genética Molecular, São Paulo, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Genetics(clinical),General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2009.0192

Reference49 articles.

1. Germline mutations in HRAS proto-oncogene cause Costello syndrome

2. The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders

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

4. Further evidence of genetic heterogeneity in Costello syndrome: involvement of the KRAS gene

5. Neurofibromatosis-Noonan syndrome: Molecular evidence of the concurrence of both disorders in a patient

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