Genotypes and phenotypes of β-thalassemia in Mediterranean populations
- Author
- KATTAMIS, C1 ; KATTAMIS, A. C1
[1] First Department of Pediatrics, Athens University, Athens, Greece - Source
Pediatric hematology and oncology. 1997, Vol 14, Num 3, pp vii-ix ; ref : 11 ref
- CODEN
- PHONEN
- ISSN
- 0888-0018
- Scientific domain
- Medical oncology; Hematology; Pediatrics
- Publisher
- Taylor & Francis, Philadelphia, PA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Epidémiologie Génotype Homme Phénotype Région méditerranéenne Thalassémie β Anémie hémolytique Hémoglobinopathie Hémopathie Maladie héréditaire
- Keyword (en)
- Epidemiology Genotype Human Phenotype Mediterranean region β-Thalassemia Hemolytic anemia Hemoglobinopathy Hemopathy Genetic disease
- Keyword (es)
- Epidemiología Genotipo Hombre Fenotipo Región mediterránea Talasemia β Anemia hemolítica Hemoglobinopatía Hemopatía Enfermedad hereditaria
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19A Diseases of red blood cells / 002B19A01 Anemias. Hemoglobinopathies
- Discipline
- Blood diseases
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 2684697
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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