Your browser doesn't support javascript.
loading
Customized Massive Parallel Sequencing Panel for Diagnosis of Pulmonary Arterial Hypertension.
Castaño, Jair Antonio Tenorio; Hernández-Gonzalez, Ignacio; Gallego, Natalia; Pérez-Olivares, Carmen; Ochoa Parra, Nuria; Arias, Pedro; Granda, Elena; Acebo, Gonzalo Gómez; Lago-Docampo, Mauro; Palomino-Doza, Julian; López Meseguer, Manuel; Del Cerro, María Jesús; Pah Consortium, Spanish; Valverde, Diana; Lapunzina, Pablo; Escribano-Subías, Pilar.
Affiliation
  • Castaño JAT; Institute of Medical and Molecular Genetics (INGEMM)-IdiPAZ, Hospital Universitario La Paz-UAM Paseo de La Castellana, 261, 28046 Madrid, Spain.
  • Hernández-Gonzalez I; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII, Melchor Fernández Almagro, 3, 28029 Madrid, Spain.
  • Gallego N; ITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability, 1000 Brussels, Belgium.
  • Pérez-Olivares C; Department of Cardiology, Hospital Universitario Río Hortega, 47012 Valladolid, Spain.
  • Ochoa Parra N; Institute of Medical and Molecular Genetics (INGEMM)-IdiPAZ, Hospital Universitario La Paz-UAM Paseo de La Castellana, 261, 28046 Madrid, Spain.
  • Arias P; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII, Melchor Fernández Almagro, 3, 28029 Madrid, Spain.
  • Granda E; ITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability, 1000 Brussels, Belgium.
  • Acebo GG; Unidad Multidisciplinar de Hipertensión Pulmonar, Servicio de Cardiología, Hospital Universitario 12 de Octubre, 28034 Madrid, Spain.
  • Lago-Docampo M; Unidad Multidisciplinar de Hipertensión Pulmonar, Servicio de Cardiología, Hospital Universitario 12 de Octubre, 28034 Madrid, Spain.
  • Palomino-Doza J; Institute of Medical and Molecular Genetics (INGEMM)-IdiPAZ, Hospital Universitario La Paz-UAM Paseo de La Castellana, 261, 28046 Madrid, Spain.
  • López Meseguer M; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII, Melchor Fernández Almagro, 3, 28029 Madrid, Spain.
  • Del Cerro MJ; ITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability, 1000 Brussels, Belgium.
  • Pah Consortium S; Institute of Medical and Molecular Genetics (INGEMM)-IdiPAZ, Hospital Universitario La Paz-UAM Paseo de La Castellana, 261, 28046 Madrid, Spain.
  • Valverde D; CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, ISCIII, Melchor Fernández Almagro, 3, 28029 Madrid, Spain.
  • Lapunzina P; ITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disability, 1000 Brussels, Belgium.
  • Escribano-Subías P; Institute of Medical and Molecular Genetics (INGEMM)-IdiPAZ, Hospital Universitario La Paz-UAM Paseo de La Castellana, 261, 28046 Madrid, Spain.
Genes (Basel) ; 11(10)2020 09 30.
Article in En | MEDLINE | ID: mdl-33007923
Subject(s)
Key words
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: High-Throughput Nucleotide Sequencing / Familial Primary Pulmonary Hypertension Type of study: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2020 Type: Article
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: High-Throughput Nucleotide Sequencing / Familial Primary Pulmonary Hypertension Type of study: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Year: 2020 Type: Article