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Genetic basis of unexplained erythrocytosis in Indian patients.
Mallik, Nabhajit; Sharma, Prashant; Kaur Hira, Jasbir; Chhabra, Sanjeev; Sreedharanunni, Sreejesh; Kumar, Narender; Naseem, Shano; Sachdeva, Man Updesh Singh; Ahluwalia, Jasmina; Malhotra, Pankaj; Varma, Neelam; Varma, Subhash; Das, Reena.
Afiliación
  • Mallik N; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sharma P; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kaur Hira J; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Chhabra S; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sreedharanunni S; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kumar N; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Naseem S; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Sachdeva MUS; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Ahluwalia J; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Malhotra P; Department of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Varma N; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Varma S; Department of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Das R; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Eur J Haematol ; 103(2): 124-130, 2019 Aug.
Article en En | MEDLINE | ID: mdl-31132167

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Policitemia / Predisposición Genética a la Enfermedad / Estudios de Asociación Genética Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Eur J Haematol Asunto de la revista: HEMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: India Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Policitemia / Predisposición Genética a la Enfermedad / Estudios de Asociación Genética Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged País/Región como asunto: Asia Idioma: En Revista: Eur J Haematol Asunto de la revista: HEMATOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: India Pais de publicación: Reino Unido