Your browser doesn't support javascript.
loading
Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients.
Papadopoulos, George; Papadopoulou, Anna; Kosma, Konstantina; Papadimitriou, Anastasios; Papaevangelou, Vassiliki; Kanaka-Gantenbein, Christina; Bountouvi, Evangelia; Kitsiou-Tzeli, Sophia.
Afiliação
  • Papadopoulos G; 3rd Department of Pediatrics, University of Athens, Medical School, University General Hospital "ATTIKON", Chaidari, Greece.
  • Papadopoulou A; 3rd Department of Pediatrics, University of Athens, Medical School, University General Hospital "ATTIKON", Chaidari, Greece. anpapado@med.uoa.gr.
  • Kosma K; Department of Medical Genetics, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
  • Papadimitriou A; 3rd Department of Pediatrics, University of Athens, Medical School, University General Hospital "ATTIKON", Chaidari, Greece.
  • Papaevangelou V; 3rd Department of Pediatrics, University of Athens, Medical School, University General Hospital "ATTIKON", Chaidari, Greece.
  • Kanaka-Gantenbein C; Division of Endocrinology, Diabetes and Metabolism, Center for Rare Paediatric Endocrine Diseases, First Department of Paediatrics, Medical School, National and Kapodistrian University of Athens, Agia Sophia Children's Hospital, Athens, Greece.
  • Bountouvi E; 3rd Department of Pediatrics, University of Athens, Medical School, University General Hospital "ATTIKON", Chaidari, Greece.
  • Kitsiou-Tzeli S; Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Eur J Pediatr ; 181(10): 3691-3700, 2022 Oct.
Article em En | MEDLINE | ID: mdl-35904599
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Noonan Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Eur J Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Grécia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Noonan Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans País/Região como assunto: Europa Idioma: En Revista: Eur J Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Grécia