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Accurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing.
Vattulainen, Sanna; Aho, Joonas; Salmenperä, Pertteli; Bruce, Siina; Tallila, Jonna; Gentile, Massimiliano; Sankelo, Marja; Laitinen, Tarja; Koskenvuo, Juha W; Alastalo, Tero-Pekka; Myllykangas, Samuel.
Afiliação
  • Vattulainen S; Pediatric Cardiology, Children's Hospital Helsinki, University of Helsinki and Helsinki University Central Hospital Helsinki, Finland.
  • Aho J; Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku Turku, Finland.
  • Salmenperä P; Blueprint Genetics Helsinki, Finland.
  • Bruce S; Blueprint Genetics Helsinki, Finland.
  • Tallila J; Blueprint Genetics Helsinki, Finland.
  • Gentile M; Blueprint Genetics Helsinki, Finland.
  • Sankelo M; Department of Internal Medicine, Tampere University Hospital Tampere, Finland.
  • Laitinen T; Department of Pulmonary Diseases and Allergology, Turku University Hospital and University of Turku Turku, Finland.
  • Koskenvuo JW; Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku Turku, Finland ; Blueprint Genetics Helsinki, Finland ; Department of Clinical Physiology and Nuclear Medicine, HUS Medical Imaging Center, Helsinki University of Central Hospital and University of Helsinki Helsin
  • Alastalo TP; Pediatric Cardiology, Children's Hospital Helsinki, University of Helsinki and Helsinki University Central Hospital Helsinki, Finland ; Blueprint Genetics Helsinki, Finland.
  • Myllykangas S; Blueprint Genetics Helsinki, Finland ; Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of Helsinki Helsinki, Finland.
Mol Genet Genomic Med ; 3(4): 354-62, 2015 Jul.
Article em En | MEDLINE | ID: mdl-26247051

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Finlândia