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Genotype-phenotype correlations
Original article
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome
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Authors

  • Guilherme Lopes Yamamoto Unidade de Genética, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Meire Aguena Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Monika Gos Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland PubMed articlesGoogle scholar articles
  • Christina Hung Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, Massachusetts, USA PubMed articlesGoogle scholar articles
  • Jacek Pilch Department of Child Neurology, Medical University of Silesia, Katowice, Poland PubMed articlesGoogle scholar articles
  • Somayyeh Fahiminiya Department of Human Genetics, McGill University, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Anna Abramowicz Department of Medical Genetics, Institute of Mother and Child, Warsaw, Poland PubMed articlesGoogle scholar articles
  • Ingrid Cristian Nemours Children's Hospital Orlando, Orlando, Florida, USA PubMed articlesGoogle scholar articles
  • Michelle Buscarilli Unidade de Genética, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Michel Satya Naslavsky Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Alexsandra C Malaquias Departamento de Endocrinologia, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Mayana Zatz Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Olaf Bodamer Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, Massachusetts, USA PubMed articlesGoogle scholar articles
  • Jacek Majewski Department of Human Genetics, McGill University, Montreal, Quebec, Canada PubMed articlesGoogle scholar articles
  • Alexander A L Jorge Departamento de Endocrinologia, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Alexandre C Pereira Instituto de Cardiologia, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Chong Ae Kim Unidade de Genética, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Maria Rita Passos-Bueno Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  • Débora Romeo Bertola Unidade de Genética, Instituto da Criança, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, São Paulo, Brazil Centro de Pesquisa sobre o Genoma Humano e Células-Tronco, Instituto de Biociências da Universidade de São Paulo, São Paulo, São Paulo, Brazil PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Débora Romeo Bertola, Unidade de Genética, Instituto da Criança do Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, Av. Dr. Enéas Carvalho de Aguiar, 647, São Paulo, SP CEP 05403-000, Brazil; debora.bertola{at}usp.br
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Citation

Yamamoto GL, Aguena M, Gos M, et al
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome
Journal of Medical Genetics 2015;52:413-421.

Publication history

  • Received January 13, 2015
  • Revised March 4, 2015
  • Accepted March 5, 2015
  • First published March 20, 2015.
Online issue publication 
October 20, 2016

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