Your browser doesn't support javascript.
loading
Exome Sequencing Analysis in Severe, Early-Onset Chronic Obstructive Pulmonary Disease.
Qiao, Dandi; Lange, Christoph; Beaty, Terri H; Crapo, James D; Barnes, Kathleen C; Bamshad, Michael; Hersh, Craig P; Morrow, Jarrett; Pinto-Plata, Victor M; Marchetti, Nathaniel; Bueno, Raphael; Celli, Bartolome R; Criner, Gerald J; Silverman, Edwin K; Cho, Michael H.
Afiliación
  • Qiao D; 1 Channing Division of Network Medicine.
  • Lange C; 2 Department of Biostatistics, Harvard School of Public Health, Boston, Massachusetts.
  • Beaty TH; 3 Johns Hopkins Bloomberg School of Public Health, and.
  • Crapo JD; 4 National Jewish Health, Denver, Colorado.
  • Barnes KC; 5 Division of Allergy and Clinical Immunology, Department of Medicine, Johns Hopkins University, Baltimore, Maryland.
  • Bamshad M; 6 Division of Genetic Medicine, Department of Pediatrics, University of Washington and Seattle Children's Hospital, Seattle, Washington.
  • Hersh CP; 1 Channing Division of Network Medicine.
  • Morrow J; 7 Division of Pulmonary and Critical Care Medicine, and.
  • Pinto-Plata VM; 1 Channing Division of Network Medicine.
  • Marchetti N; 8 Department of Critical Care Medicine and Pulmonary Disease, Baystate Medical Center, Springfield, Massachusetts.
  • Bueno R; 9 Department of Thoracic Medicine and Surgery, and.
  • Celli BR; 10 Division of Thoracic Surgery, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
  • Criner GJ; 7 Division of Pulmonary and Critical Care Medicine, and.
  • Silverman EK; 11 Division of Pulmonary and Critical Care Medicine Temple University School of Medicine, Philadelphia, Pennsylvania.
  • Cho MH; 1 Channing Division of Network Medicine.
Am J Respir Crit Care Med ; 193(12): 1353-63, 2016 06 15.
Article en En | MEDLINE | ID: mdl-26736064
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Deficiencia de alfa 1-Antitripsina / Predisposición Genética a la Enfermedad / Enfermedad Pulmonar Obstructiva Crónica / Estudio de Asociación del Genoma Completo / Exoma Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Deficiencia de alfa 1-Antitripsina / Predisposición Genética a la Enfermedad / Enfermedad Pulmonar Obstructiva Crónica / Estudio de Asociación del Genoma Completo / Exoma Tipo de estudio: Prognostic_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: America do norte Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2016 Tipo del documento: Article Pais de publicación: Estados Unidos